|
humans |
26 |
|
female |
24 |
|
pregnancy |
20 |
|
adult |
19 |
|
prenatal diagnosis |
17 |
|
chinese |
12 |
|
hong kong |
12 |
|
gestational age |
10 |
|
ultrasound |
10 |
|
down syndrome |
9 |
|
homozygote |
9 |
|
middle aged |
9 |
|
phenotyping |
8 |
|
predictive value of tests |
8 |
|
prenatal exome |
8 |
|
ultrasonography, prenatal - methods |
8 |
|
variants of unknown clinical significance |
8 |
|
beta-thalassemia - diagnosis - genetics |
7 |
|
case-control studies |
7 |
|
infant |
7 |
|
male |
7 |
|
maternal age |
7 |
|
thalassaemia |
7 |
|
ultrasonography |
7 |
|
attitude |
6 |
|
comparative genomic hybridization |
6 |
|
down's syndrome |
6 |
|
fetal blood |
6 |
|
hydrops fetalis |
6 |
|
infant, newborn |
6 |
|
nuchal translucency |
6 |
|
pregnancy - blood |
6 |
|
pregnancy trimester, first |
6 |
|
pregnancy trimester, first - blood |
6 |
|
preimplantation diagnosis |
6 |
|
prenatal diagnosis - methods |
6 |
|
retrospective studies |
6 |
|
twins |
6 |
|
alpha-thalassemia - diagnosis - genetics |
5 |
|
alport's syndrome |
5 |
|
anti-mullerian hormone |
5 |
|
anti-mullerian hormone - blood |
5 |
|
asian continental ancestry group - genetics |
5 |
|
beta-thalassemia - blood - immunology - therapy |
5 |
|
cord blood stem cell |
5 |
|
dna mutational analysis |
5 |
|
down syndrome - blood |
5 |
|
esophageal leiomyoma |
5 |
|
feasibility studies |
5 |
|
fertilization in vitro |
5 |
|
fetal diseases - ultrasonography |
5 |
|
fetal hemoglobin |
5 |
|
fetal hemoglobin - biosynthesis |
5 |
|
fetal tissue transplantation |
5 |
|
graft survival |
5 |
|
hematopoietic stem cell transplantation |
5 |
|
histocompatibility testing |
5 |
|
imaging, three-dimensional |
5 |
|
karyotyping |
5 |
|
organ size |
5 |
|
pediatrics |
5 |
|
placenta |
5 |
|
screening |
5 |
|
sensitivity and specificity |
5 |
|
transplantation |
5 |
|
transplantation, homologous |
5 |
|
α-thalassemia |
5 |
|
β-thalassemia major |
5 |
|
acceptance |
4 |
|
adaptor proteins, signal transducing - genetics |
4 |
|
adolescent |
4 |
|
afp |
4 |
|
aged |
4 |
|
alpha-fetoprotein |
4 |
|
amniotic fluid |
4 |
|
amp-activated protein kinases |
4 |
|
aortic stenosis |
4 |
|
array comparative genomic hybridization |
4 |
|
array comparative genomic hybridization (acgh) |
4 |
|
art |
4 |
|
asian continental ancestry group |
4 |
|
asians |
4 |
|
assisted reproduction |
4 |
|
autism spectrum disorder (asd) |
4 |
|
biological markers - blood |
4 |
|
blood flow velocity |
4 |
|
bowel |
4 |
|
candidate cancer genes |
4 |
|
carcinoma, squamous cell - genetics |
4 |
|
cardiomegaly |
4 |
|
cervical cancer |
4 |
|
china - ethnology |
4 |
|
chinese couple |
4 |
|
chorionic gonadotropin, beta subunit, human - blood |
4 |
|
chromosomal microarray |
4 |
|
chromosomal proteins, non-histone - genetics |
4 |
|
chromosome 17p13.3 |
4 |
|
chromosome aberration |
4 |
|
chromosome deletion |
4 |
|
chromosome, human, y |
4 |
|
chromosomes, human, pair 5 - genetics |
4 |
|
concern |
4 |
|
copy number variations (cnvs) |
4 |
|
counseling |
4 |
|
cryopreservation |
4 |
|
cysts - congenital - ultrasonography |
4 |
|
dna methylation |
4 |
|
dna, neoplasm - genetics |
4 |
|
dna, viral - genetics |
4 |
|
dna-directed dna polymerase - genetics |
4 |
|
down syndrome - blood - diagnosis |
4 |
|
down syndrome - diagnosis |
4 |
|
dpp10 |
4 |
|
duplication cyst |
4 |
|
dysmorphism |
4 |
|
embryo transfer |
4 |
|
embryo, mammalian |
4 |
|
expanded carrier screening |
4 |
|
fet |
4 |
|
fetal anemia |
4 |
|
fetal diseases - embryology - ultrasonography |
4 |
|
first trimester |
4 |
|
frozen embryo transfer |
4 |
|
frozen-thawed embryo transfer |
4 |
|
gene amplification |
4 |
|
gene dosage |
4 |
|
genetic predisposition to disease |
4 |
|
hb-bart's disease |
4 |
|
hcg |
4 |
|
homozygous α 0-thalassemia |
4 |
|
human chorionic gonadotrophin |
4 |
|
icsi |
4 |
|
ileal diseases - congenital - ultrasonography |
4 |
|
ileum |
4 |
|
ileum - abnormalities |
4 |
|
imprinting |
4 |
|
in-vitro fertilization |
4 |
|
infertility, male |
4 |
|
intracytoplasmic sperm injection |
4 |
|
ivf |
4 |
|
ivf-embryo transfer |
4 |
|
microcephaly |
4 |
|
microduplication |
4 |
|
middle cerebral artery |
4 |
|
multienzyme complexes - genetics |
4 |
|
non-invasive prenatal diagnosis |
4 |
|
nt |
4 |
|
nuclear proteins - genetics |
4 |
|
papillomaviridae - genetics |
4 |
|
papillomavirus infections - complications - enzymology - genetics |
4 |
|
papp-a |
4 |
|
paternal upd |
4 |
|
polymerase chain reaction |
4 |
|
polymerase chain reaction - methods |
4 |
|
pregnancy complications, hematologic - diagnosis |
4 |
|
pregnancy outcome |
4 |
|
pregnancy-associated plasma protein-a - metabolism |
4 |
|
preimplantation genetic testing |
4 |
|
prenatal screening |
4 |
|
prenatal ultrasonography |
4 |
|
prkaa1 |
4 |
|
prospective studies |
4 |
|
protein-serine-threonine kinases - genetics |
4 |
|
questionnaires |
4 |
|
reverse transcriptase polymerase chain reaction - methods |
4 |
|
semi-quantitative fluorescent differential pcr |
4 |
|
sperm injections, intracytoplasmic |
4 |
|
survey |
4 |
|
thalassemia - diagnosis - genetics |
4 |
|
ultrasonography, prenatal |
4 |
|
ultrasonography, prenatal - methods - standards |
4 |
|
uniparental sisomy |
4 |
|
upd19 |
4 |
|
uterine cervical neoplasms - enzymology - genetics - virology |
4 |
|
17p13.3 copy number gain |
3 |
|
3d ultrasound |
3 |
|
adenomyosis |
3 |
|
agenesis of the corpus callosum |
3 |
|
alleles |
3 |
|
alpha-fetoproteins - analysis |
3 |
|
alpha-thalassemia - blood - diagnosis |
3 |
|
alpha-thalassemia - blood - diagnosis - genetics |
3 |
|
alpha-thalassemia - complications - ultrasonography |
3 |
|
alpha-thalassemia - embryology - ultrasonography |
3 |
|
alpha-thalassemia - genetics - physiopathology - ultrasonography |
3 |
|
alpha-thalassemia - genetics - ultrasonography |
3 |
|
alpha-thalassemia - pathology - ultrasonography |
3 |
|
alpha-thalassemia - ultrasonography |
3 |
|
analysis of variance |
3 |
|
aneuploidy |
3 |
|
anxiety |
3 |
|
anxiety - etiology |
3 |
|
aorta, thoracic - physiopathology - ultrasonography |
3 |
|
array cgh |
3 |
|
autism |
3 |
|
autosome translocation |
3 |
|
beta-globins - genetics |
3 |
|
beta-thalassemia - blood - diagnosis |
3 |
|
biological markers - analysis - blood |
3 |
|
biological markers - urine |
3 |
|
blood transfusion |
3 |
|
carbocyanines - diagnostic use |
3 |
|
cardiomegaly - complications - ultrasonography |
3 |
|
cardiomegaly - ultrasonography |
3 |
|
cervical vertebrae - abnormalities - ultrasonography |
3 |
|
charge syndrome |
3 |
|
chorionic gonadotropin - blood |
3 |
|
chorionic gonadotropin, beta subunit, human - analysis - blood |
3 |
|
chorionic gonadotropin, beta subunit, human - urine |
3 |
|
chromosome aberrations |
3 |
|
chromosome mapping |
3 |
|
coffin-siris syndrome |
3 |
|
computer |
3 |
|
congenital malformations |
3 |
|
coronary circulation |
3 |
|
cost effectiveness |
3 |
|
cost effectiveness analysis |
3 |
|
cost saving |
3 |
|
cost-benefit analysis |
3 |
|
craniofacial defects |
3 |
|
cystic adenomatoid malformation of lung, congenital |
3 |
|
decision trees |
3 |
|
deoxycytosine nucleotides - diagnostic use |
3 |
|
developmental delay |
3 |
|
diaphragmatic hernia |
3 |
|
dna - analysis |
3 |
|
doppler |
3 |
|
down syndrome - diagnosis - embryology - ethnology |
3 |
|
dysostoses - ultrasonography |
3 |
|
endometriosis |
3 |
|
endometriosis - diagnosis - pathology |
3 |
|
false negative reactions |
3 |
|
false positive reactions |
3 |
|
family health |
3 |
|
fathers |
3 |
|
fetal diseases - blood - diagnosis - genetics |
3 |
|
fetal diseases - diagnosis |
3 |
|
fetal diseases - diagnosis - enzymology - genetics |
3 |
|
fetal diseases - diagnosis - ethnology - urine |
3 |
|
fetal diseases - pathology - ultrasonography |
3 |
|
fetus |
3 |
|
fetus - abnormalities |
3 |
|
fetus - pathology |
3 |
|
fluorescent antibody technique |
3 |
|
gastric dilatation - ultrasonography |
3 |
|
gene deletion |
3 |
|
genetic counseling and training |
3 |
|
genome-wide dna methylation microarray |
3 |
|
health professionals |
3 |
|
hemoglobins - analysis |
3 |
|
hemoglobins - metabolism |
3 |
|
hernia, diaphragmatic - ultrasonography |
3 |
|
heterozygote |
3 |
|
hong kong - epidemiology |
3 |
|
hysterectomy |
3 |
|
information provision |
3 |
|
informative snp |
3 |
|
interactive program |
3 |
|
intrauterine |
3 |
|
jarcho-levin syndrome |
3 |
|
linear models |
3 |
|
mass screening |
3 |
|
maternal-fetal relations |
3 |
|
maternal-plasma dna |
3 |
|
medical records |
3 |
|
microdeletion |
3 |
|
middle cerebral artery - physiopathology - ultrasonography |
3 |
|
middle cerebral artery - ultrasonography |
3 |
|
minor anomalies |
3 |
|
morphogenesis |
3 |
|
mothers - psychology |
3 |
|
mutation |
3 |
|
normal distribution |
3 |
|
observer variation |
3 |
|
outcome assessment (health care) |
3 |
|
parental decisions |
3 |
|
paternal mutation |
3 |
|
patient satisfaction |
3 |
|
pelvic neoplasms - diagnosis - pathology |
3 |
|
peptide fragments - urine |
3 |
|
placenta - pathology - ultrasonography |
3 |
|
placenta - physiopathology - ultrasonography |
3 |
|
placenta - ultrasonography |
3 |
|
polymorphism, single nucleotide |
3 |
|
pregnancy complications, hematologic - blood - diagnosis |
3 |
|
pregnancy termination |
3 |
|
pregnancy trimester, second |
3 |
|
pregnancy, high-risk |
3 |
|
pregnancy-associated plasma protein-a - analysis |
3 |
|
preimplantation genetic diagnosis |
3 |
|
prenatal diagnosis - economics - methods |
3 |
|
prenatal diagnosis - methods - statistics & numerical data |
3 |
|
prenatal test |
3 |
|
prenatally-diagnosed tumours |
3 |
|
prognosis |
3 |
|
psychiatric status rating scales |
3 |
|
pyruvate kinase - deficiency - genetics |
3 |
|
pyruvate kinase deficiency |
3 |
|
rapid aneuploidy diagnosis |
3 |
|
reproducibility of results |
3 |
|
ribs - abnormalities - ultrasonography |
3 |
|
risk factors |
3 |
|
scoliosis - ultrasonography |
3 |
|
second trimester |
3 |
|
serum screening |
3 |
|
sex chromosome aneuploidy |
3 |
|
site |
3 |
|
spine - abnormalities - ultrasonography |
3 |
|
split hand malformation |
3 |
|
spondylocostal dysostosis |
3 |
|
stomach |
3 |
|
thalassemia - blood - diagnosis |
3 |
|
thoracic vertebrae - abnormalities - ultrasonography |
3 |
|
three-dimensional ultrasound |
3 |
|
treatment outcome |
3 |
|
urinary gonadotrophin peptide (ugp) |
3 |
|
uterine anomaly |
3 |
|
uterine neoplasms - diagnosis - pathology |
3 |
|
uterus - abnormalities - pathology |
3 |
|
vascularity |
3 |
|
volume |
3 |
|
x |
3 |
|
x chromosome inactivation |
3 |
|
α-thalassaemia |
3 |
|
α0-thalassemia |
3 |
|
5p deletion syndrome |
2 |
|
abnormalities, multiple - genetics |
2 |
|
abnormalities, multiple - pathology - ultrasonography |
2 |
|
abortion, eugenic |
2 |
|
abortion, induced |
2 |
|
abortion, spontaneous - epidemiology |
2 |
|
acgh |
2 |
|
advanced age |
2 |
|
alkaline phosphatase |
2 |
|
alpha-thalassaemia |
2 |
|
alpha-thalassemia - blood - epidemiology - genetics - metabolism |
2 |
|
alpha-thalassemia - complications - embryology |
2 |
|
alpha-thalassemia - complications - embryology - genetics - ultrasonography |
2 |
|
alpha-thalassemia - diagnosis - embryology |
2 |
|
alpha-thalassemia - genetics - physiopathology |
2 |
|
amniocentesis |
2 |
|
amniocentesis - adverse effects |
2 |
|
aneuploidy screening |
2 |
|
animals |
2 |
|
antibodies, monoclonal - immunology |
2 |
|
antibody specificity |
2 |
|
aorta - physiopathology - ultrasonography |
2 |
|
ascites - ultrasonography |
2 |
|
asian |
2 |
|
assisted-reproduction technology |
2 |
|
b-lymphocytes - immunology |
2 |
|
beta-thalassemia - genetics |
2 |
|
blood group antigens - genetics - immunology |
2 |
|
blood grouping and crossmatching |
2 |
|
bone neoplasms - blood |
2 |
|
carcinoma, squamous cell - genetics - virology |
2 |
|
cardiac function |
2 |
|
cardiovascular abnormalities - ultrasonography |
2 |
|
cd34 + cells |
2 |
|
cell culture techniques |
2 |
|
cell culture techniques - methods |
2 |
|
cell-free dna screening |
2 |
|
cells, cultured |
2 |
|
cesarean section |
2 |
|
cfdna |
2 |
|
china |
2 |
|
chorionic villi |
2 |
|
chorionic villi sampling |
2 |
|
chorionic villi sampling - methods |
2 |
|
chromosomes, human, pair 9 |
2 |
|
cleft palate - ultrasonography |
2 |
|
cohort studies |
2 |
|
confidence intervals |
2 |
|
congenital |
2 |
|
congenital abnormalities - diagnosis - embryology - ultrasonography |
2 |
|
congenital dyserythropoietic anemia |
2 |
|
conjoined twins |
2 |
|
cri‐du‐chat syndrome |
2 |
|
cystic adenomatoid malformation of lung |
2 |
|
cytogenetic analysis |
2 |
|
detection rate |
2 |
|
diagnosis |
2 |
|
diagnosis, differential |
2 |
|
diastole |
2 |
|
doppler study |
2 |
|
down syndrome - diagnosis - embryology - ultrasonography |
2 |
|
down syndrome - diagnosis - ultrasonography |
2 |
|
down syndrome - etiology |
2 |
|
down syndrome - ultrasonography |
2 |
|
drug combinations |
2 |
|
drugs, chinese herbal - adverse effects - isolation & purification |
2 |
|
early pregnancy |
2 |
|
echogenic bowel |
2 |
|
edema - ultrasonography |
2 |
|
electrocoagulation |
2 |
|
erythrocyte indices |
2 |
|
erythrocytes - immunology |
2 |
|
ethnic origin |
2 |
|
factor viii - genetics |
2 |
|
fetal abnormalities |
2 |
|
fetal abnormality |
2 |
|
fetal blood - chemistry - metabolism |
2 |
|
fetal death - epidemiology |
2 |
|
fetal development |
2 |
|
fetal diseases - diagnosis - genetics |
2 |
|
fetal diseases - diagnosis - therapy |
2 |
|
fetal diseases - embryology |
2 |
|
fetal growth retardation - physiopathology |
2 |
|
fetal heart |
2 |
|
fetal heart - physiopathology |
2 |
|
fetal heart - ultrasonography |
2 |
|
fetal membranes, premature rupture |
2 |
|
fetal movement |
2 |
|
fetal structural abnormalities |
2 |
|
fetofetal transfusion - diagnosis - therapy |
2 |
|
fetus - anatomy & histology |
2 |
|
forecasting |
2 |
|
gender |
2 |
|
genetic diseases, inborn - diagnosis - epidemiology - prevention & control |
2 |
|
genetic linkage |
2 |
|
genetic testing |
2 |
|
genotype |
2 |
|
globins - genetics |
2 |
|
haemoglobin (hb) bart's |
2 |
|
haemoglobin bart's disease |
2 |
|
haemolytic disease of the newborn |
2 |
|
haemopoietic primitive cell |
2 |
|
hb bart's |
2 |
|
hb h hydrops |
2 |
|
hemivertebra |
2 |
|
hemoglobin h - genetics |
2 |
|
hemoglobins - analysis - metabolism |
2 |
|
hemoglobins, abnormal - analysis - metabolism |
2 |
|
hemophilia a - diagnosis - genetics |
2 |
|
hemophilia a - diagnosis - prevention & control |
2 |
|
hemophilia b - diagnosis - prevention & control |
2 |
|
herbal medicine |
2 |
|
heterozygote detection |
2 |
|
holoprosencephaly - ultrasonography |
2 |
|
human serum albumin |
2 |
|
hydrops |
2 |
|
hydrops fetalis - blood - diagnosis - genetics |
2 |
|
hydrops fetalis - etiology - ultrasonography |
2 |
|
hypophosphatasia |
2 |
|
image processing, computer-assisted - methods |
2 |
|
imaging, three-dimensional - methods |
2 |
|
intestines - embryology - ultrasonography |
2 |
|
intrauterine transfusion |
2 |
|
introns |
2 |
|
isoantibodies - genetics - immunology |
2 |
|
knowledge and acceptance |
2 |
|
krüppel-like factor 1 (klf1) gene mutations |
2 |
|
leukaemias |
2 |
|
leukemia - immunology |
2 |
|
limb deformities, congenital - embryology - etiology - pathology |
2 |
|
limb reduction defect |
2 |
|
lumbar vertebrae - abnormalities - embryology - ultrasonography |
2 |
|
lung diseases |
2 |
|
lymphangioma, cystic - ultrasonography |
2 |
|
ma6 |
2 |
|
maternal health services - statistics & numerical data |
2 |
|
maternal plasma |
2 |
|
meconium peritonitis |
2 |
|
middle cerebral artery - embryology - physiopathology - ultrasonography |
2 |
|
molecular defect |
2 |
|
molecular diagnosis |
2 |
|
monoclonal antibody |
2 |
|
mosaic variegated aneuploidy |
2 |
|
multiple pregnancy |
2 |
|
muscular dystrophies - diagnosis - prevention & control |
2 |
|
nasal bone |
2 |
|
nasal bone - embryology - ultrasonography |
2 |
|
nasal bones |
2 |
|
neck - embryology - ultrasonography |
2 |
|
neonatal anemia |
2 |
|
newborn |
2 |
|
non-invasive prenatal testing |
2 |
|
nuchal scan |
2 |
|
nuchal translucency measurement |
2 |
|
nuchal translucency ultrasound |
2 |
|
nucleic acid hybridization |
2 |
|
omphalopagus |
2 |
|
outcome |
2 |
|
papillomaviridae - classification - isolation & purification |
2 |
|
pathogenesis |
2 |
|
patient acceptance of health care |
2 |
|
perinatal lethal form of hypophosphatasia |
2 |
|
pharmaceutical preparations - adverse effects |
2 |
|
pilot projects |
2 |
|
placenta - pathology |
2 |
|
plants, medicinal |
2 |
|
polyhydramnios |
2 |
|
polyhydramnios - etiology - therapy |
2 |
|
polymorphism, restriction fragment length |
2 |
|
postmortem mri |
2 |
|
pre-implantation genetic diagnosis |
2 |
|
pregnancy - immunology |
2 |
|
pregnancy complications, hematologic - ultrasonography |
2 |
|
pregnancy complications, neoplastic - blood |
2 |
|
pregnancy reduction, multifetal - methods |
2 |
|
pregnancy, twin |
2 |
|
prenatal |
2 |
|
prevalence |
2 |
|
probability |
2 |
|
pterygium syndrome |
2 |
|
pulmonary artery - physiopathology - ultrasonography |
2 |
|
randomization |
2 |
|
red cell antibodies |
2 |
|
reference values |
2 |
|
risk of atypical aneuploidies |
2 |
|
roc curve |
2 |
|
sacrococcygeal region |
2 |
|
selective reduction |
2 |
|
sequence analysis, dna |
2 |
|
sex |
2 |
|
spinal dysraphism - ultrasonography |
2 |
|
spine - ultrasonography |
2 |
|
statistics, nonparametric |
2 |
|
syndrome |
2 |
|
teratogenicity |
2 |
|
teratoma - blood |
2 |
|
thalassemia - diagnosis - prevention & control |
2 |
|
thermocoagulation |
2 |
|
thorax - embryology - ultrasonography |
2 |
|
three-dimensional ultrasonography |
2 |
|
time factors |
2 |
|
transfusion |
2 |
|
triplets |
2 |
|
trisomy |
2 |
|
tsalp gene |
2 |
|
twins, conjoined |
2 |
|
ultrasonography, doppler |
2 |
|
ultrasonography, doppler, color |
2 |
|
ultrasonography, doppler, pulsed |
2 |
|
umbilical cord blood |
2 |
|
uterine cervical neoplasms - genetics - virology |
2 |
|
vhl gene |
2 |
|
vhl mutations |
2 |
|
von hippel-lindau disease - genetics |
2 |
|
von hippel-lindau syndrome |
2 |
|
von hippel-lindau tumor suppressor protein - genetics |
2 |
|
vulvar neoplasms - genetics - virology |
2 |
|
whole-genome array comparative genomic hybridization |
2 |
|
x chromosome |
2 |
|
α thalassaemia |
2 |
|
α‐thalassaemia‐1 |
2 |
|
β-thalassaemia |
2 |
|
εγδβ-thalassemia (εγδβ-thal) |
2 |
|
11-14 weeks gestation |
1 |
|
2d ultrasound |
1 |
|
3d ultrasonography |
1 |
|
abnormalities, multiple - pathology |
1 |
|
abnormalities, multiple - ultrasonography |
1 |
|
abnormalities,-multiple-genetics |
1 |
|
aborted fetus - pathology |
1 |
|
abortion, therapeutic |
1 |
|
acrocephalosyndactylia - diagnosis - genetics |
1 |
|
alpha-thalassemia - blood |
1 |
|
alpha-thalassemia - blood - genetics - ultrasonography |
1 |
|
alpha-thalassemia - diagnosis - genetics - physiopathology |
1 |
|
amniocentesis - psychology |
1 |
|
amnion - abnormalities - ultrasonography |
1 |
|
amniotic fluid - chemistry |
1 |
|
amniotic fluid - cytology |
1 |
|
anaemia |
1 |
|
anal atresia |
1 |
|
anencephaly |
1 |
|
anencephaly - diagnosis |
1 |
|
aneuploidy testing |
1 |
|
antibodies - blood |
1 |
|
antibodies, monoclonal - diagnostic use |
1 |
|
anus, imperforate - ultrasonography |
1 |
|
aorta - physiology |
1 |
|
aorta, abdominal - embryology - physiology |
1 |
|
apert syndrome |
1 |
|
arrhythmia |
1 |
|
arrhythmias, cardiac - diagnosis |
1 |
|
artifacts |
1 |
|
ascites - diagnosis - ultrasonography |
1 |
|
autopsy |
1 |
|
base sequence |
1 |
|
betamethasone |
1 |
|
biometry |
1 |
|
biometry - methods |
1 |
|
birth-weight prediction |
1 |
|
blood flow velocity - physiology |
1 |
|
blood group incompatibility - immunology |
1 |
|
blood volume |
1 |
|
bradycardia - etiology |
1 |
|
brain |
1 |
|
brain - abnormalities |
1 |
|
caml |
1 |
|
cardiac blood flow |
1 |
|
cardiac output |
1 |
|
cardiac tumors |
1 |
|
cardiomegaly - congenital - ultrasonography |
1 |
|
cartilage-hair hypoplasia |
1 |
|
central nervous system - abnormalities |
1 |
|
cerebral cortex - abnormalities - ultrasonography |
1 |
|
chinese population |
1 |
|
chorionic villi - chemistry |
1 |
|
chromosomal abnormality |
1 |
|
chromosome aberrations - diagnosis |
1 |
|
chromosome banding |
1 |
|
chromosome disorders |
1 |
|
chromosome disorders - diagnosis - genetics |
1 |
|
chromosome duplication |
1 |
|
chromosome-aberrations-genetics |
1 |
|
chromosomes, human, 16-18 |
1 |
|
chromosomes, human, pair 13 |
1 |
|
chromosomes, human, pair 13 - genetics |
1 |
|
chromosomes, human, pair 18 |
1 |
|
chromosomes, human, pair 18 - genetics |
1 |
|
chromosomes, human, pair 2 |
1 |
|
chromosomes, human, pair 21 - genetics |
1 |
|
chromosomes, human, pair 6 |
1 |
|
chromosomes, human, pair 7 |
1 |
|
chromosomes, human, y - genetics |
1 |
|
chromosomes,-human,-pair-17 |
1 |
|
chylothorax |
1 |
|
chylothorax - complications - congenital - diagnosis - surgery |
1 |
|
chylothorax - congenital - diagnosis |
1 |
|
chylothorax - diagnosis - drug therapy - embryology |
1 |
|
chylous ascites - diagnosis - ultrasonography |
1 |
|
cleft lip |
1 |
|
cleft lip - embryology - ultrasonography |
1 |
|
cleft palate |
1 |
|
cleft palate - embryology - ultrasonography |
1 |
|
comparative genomic hybridization - methods |
1 |
|
congenital chylothorax |
1 |
|
congenital heart defect |
1 |
|
congenital heart disease |
1 |
|
congenital pleural effusion |
1 |
|
cordocentesis |
1 |
|
cordocentesis - adverse effects - methods |
1 |
|
coronary vessel anomalies - ultrasonography |
1 |
|
corticosteroid therapy |
1 |
|
cricetinae |
1 |
|
culture failure |
1 |
|
cystic adenomatoid malformation |
1 |
|
cytogenetics |
1 |
|
da-dapi |
1 |
|
decision making |
1 |
|
diagnosis and monitoring |
1 |
|
dilatation, pathologic - ultrasonography |
1 |
|
discrepant findings |
1 |
|
dna - blood |
1 |
|
dna - chemistry - genetics |
1 |
|
dna - genetics |
1 |
|
dna primers |
1 |
|
doppler ultrasonography |
1 |
|
down syndrome - blood - diagnosis - embryology |
1 |
|
down syndrome - diagnosis - genetics |
1 |
|
down syndrome - diagnosis - genetics - psychology |
1 |
|
ebstein anomaly |
1 |
|
echocardiography |
1 |
|
echocardiography, doppler - methods |
1 |
|
echocardiography, three-dimensional - methods |
1 |
|
echoencephalography |
1 |
|
edema |
1 |
|
electrocardiography |
1 |
|
embryonic |
1 |
|
embryonic development - physiology |
1 |
|
endoribonucleases - genetics |
1 |
|
epidermolysis bullosa, junctional - diagnosis - genetics |
1 |
|
erythroblastosis, fetal - immunology |
1 |
|
erythrocytes - chemistry |
1 |
|
erythroid cells |
1 |
|
erythroid precursor cells |
1 |
|
exomphalos |
1 |
|
exons - genetics |
1 |
|
extremities - embryology - ultrasonography |
1 |
|
face-abnormalities |
1 |
|
facial bones - abnormalities |
1 |
|
fatal outcome |
1 |
|
femur - embryology - ultrasonography |
1 |
|
fetal |
1 |
|
fetal blood - chemistry |
1 |
|
fetal chylothorax |
1 |
|
fetal congenital heart block |
1 |
|
fetal development - physiology |
1 |
|
fetal diseases - blood - diagnosis |
1 |
|
fetal diseases - diagnosis - drug therapy |
1 |
|
fetal diseases - diagnosis - epidemiology - genetics |
1 |
|
fetal diseases - diagnosis - genetics - psychology |
1 |
|
fetal diseases - diagnosis - ultrasonography |
1 |
|
fetal diseases - diagnosis- ultrasonography |
1 |
|
fetal diseases - physiopathology |
1 |
|
fetal diseases - surgery |
1 |
|
fetal diseases - ultrastructure |
1 |
|
fetal echocardiography |
1 |
|
fetal globin |
1 |
|
fetal growth restriction |
1 |
|
fetal growth retardation - complications |
1 |
|
fetal heart - embryology - physiopathology - ultrasonography |
1 |
|
fetal hemoglobin - genetics - immunology |
1 |
|
fetal hydranencephaly |
1 |
|
fetal lung lesion |
1 |
|
fetal monitoring - methods |
1 |
|
fetal volume |
1 |
|
fetus - metabolism |
1 |
|
fetus - surgery |
1 |
|
fgfr3 gene |
1 |
|
fibroma - ultrasonography |
1 |
|
fingers - ultrasonography |
1 |
|
fish |
1 |
|
folate |
1 |
|
folic acid - blood |
1 |
|
follow-up studies |
1 |
|
fractional thigh volume |
1 |
|
gene duplication |
1 |
|
gene expression regulation, developmental |
1 |
|
general cytogenetics |
1 |
|
genetic counseling |
1 |
|
genetic screening - methods |
1 |
|
genetic testing - psychology |
1 |
|
globin |
1 |
|
globins - analysis - immunology |
1 |
|
globins - genetics - immunology |
1 |
|
glycophorin - immunology |
1 |
|
hand |
1 |
|
hb bart's (γ4) disease |
1 |
|
heart |
1 |
|
heart block - diagnosis |
1 |
|
heart defects, congenital - classification - ultrasonography |
1 |
|
heart defects, congenital - complications - ultrasonography |
1 |
|
heart defects, congenital - embryology - physiopathology - ultrasonography |
1 |
|
heart defects, congenital - ultrasonography |
1 |
|
heart neoplasms - ultrasonography |
1 |
|
heart rate, fetal |
1 |
|
heart septal defects - ultrasonography |
1 |
|
heart septal defects, ventricular - ultrasonography |
1 |
|
heart valves - embryology |
1 |
|
heart ventricles - abnormalities |
1 |
|
heart ventricles - embryology - ultrasonography |
1 |
|
hemangioma - blood - complications - pathology |
1 |
|
hemangioma, cavernous - ultrasonography |
1 |
|
hemoglobinopathies - embryology - physiopathology |
1 |
|
hemoglobins, abnormal |
1 |
|
hemoglobins, abnormal - analysis |
1 |
|
hemoglobins, abnormal - analysis - immunology |
1 |
|
hernia, diaphragmatic - complications - ultrasonography |
1 |
|
hernia, umbilical - ultrasonography |
1 |
|
heterokaryotype |
1 |
|
histology |
1 |
|
holoprosencephaly |
1 |
|
holoprosencephaly - diagnosis - ultrasonography |
1 |
|
humerus - embryology - ultrasonography |
1 |
|
hydranencephaly |
1 |
|
hydranencephaly - etiology |
1 |
|
hydronephrosis - congenital - diagnosis - epidemiology |
1 |
|
hydrops fetalis - blood - diagnosis - epidemiology - etiology |
1 |
|
hydrops fetalis - diagnosis |
1 |
|
hydrops fetalis - diagnosis - etiology |
1 |
|
hypotelorism |
1 |
|
hypothyroidism |
1 |
|
image processing, computer-assisted - instrumentation - methods |
1 |
|
imaging, three-dimensional - instrumentation - methods |
1 |
|
in situ hybridization, fluorescence |
1 |
|
in situ hybridization, fluorescence - economics - utilization |
1 |
|
incidental findings |
1 |
|
inhibin-a |
1 |
|
inhibins - blood |
1 |
|
intracranial hemorrhages - ultrasonography |
1 |
|
intrauterine growth retardation |
1 |
|
introns - genetics |
1 |
|
invitro |
1 |
|
karyotyping - methods |
1 |
|
kidney - abnormalities |
1 |
|
laminin - genetics |
1 |
|
laser-doppler flowmetry |
1 |
|
limb |
1 |
|
limb deformities, congenital - etiology - ultrasonography |
1 |
|
limb reduction |
1 |
|
limb-deformities,-congenital |
1 |
|
long-term culture |
1 |
|
low risk population |
1 |
|
maternal exposure - adverse effects |
1 |
|
maternal smoking |
1 |
|
mckusick type |
1 |
|
megalourethra |
1 |
|
metaphase - genetics |
1 |
|
metaphyseal chondrodysplasia |
1 |
|
middle cerebral artery - physiopathology |
1 |
|
molecular beacon |
1 |
|
molecular diagnostic techniques |
1 |
|
molecular sequence data |
1 |
|
mosaic trisomy 21 |
1 |
|
mosaicism |
1 |
|
mouth abnormalities - ultrasonography |
1 |
|
multiplanar |
1 |
|
multiple gestation |
1 |
|
natal diagnosis |
1 |
|
neural tube defect |
1 |
|
neural tube defects |
1 |
|
neural tube defects - diagnosis |
1 |
|
neural tube defects - diagnosis - epidemiology - genetics |
1 |
|
non-paternity |
1 |
|
noninvasive |
1 |
|
nucleic acid heteroduplexes - genetics |
1 |
|
obstetrics: diagnostic ultrasound and prenatal diagnosis |
1 |
|
odds ratio |
1 |
|
ok-432 |
1 |
|
osteochondrodysplasias - genetics |
1 |
|
outflow tract |
1 |
|
ovarian cysts - blood - complications |
1 |
|
par2 |
1 |
|
partial monosomy 6q |
1 |
|
partial trisomy 7q |
1 |
|
pcr |
1 |
|
penis - abnormalities - ultrasonography |
1 |
|
perinatal findings |
1 |
|
phantom |
1 |
|
picibanil - administration & dosage |
1 |
|
placenta diseases - blood - complications - pathology |
1 |
|
placental pathology |
1 |
|
plasma dna |
1 |
|
platyspondyly lethal skeletal dysplasia |
1 |
|
pleuroamniotic shunt |
1 |
|
pleurodesis - methods |
1 |
|
polyhydramnios - complications |
1 |
|
polyhydramnios - etiology - surgery - ultrasonography |
1 |
|
polymerase chain reaction - economics - utilization |
1 |
|
pregnancy complications |
1 |
|
pregnancy complications - genetics |
1 |
|
pregnancy complications, neoplastic - blood - pathology |
1 |
|
pregnancy reduction, multifetal |
1 |
|
pregnancy trimester, third |
1 |
|
pregnancy, high-risk - blood |
1 |
|
pregnancy-associated plasma protein a |
1 |
|
prenatal care |
1 |
|
prenatal cytogenetics |
1 |
|
prenatal diagnosis (pnd) |
1 |
|
prenatal diagnosis - psychology |
1 |
|
prenatal echocardiography |
1 |
|
prenatal exposure delayed effects |
1 |
|
prenatal ultrasound |
1 |
|
proboscis |
1 |
|
pulmonary veins - abnormalities - ultrasonography |
1 |
|
pulsed doppler velocimetry |
1 |
|
qf-pcr |
1 |
|
quality of life |
1 |
|
radioisotope renography |
1 |
|
rapid aneuploidy screening |
1 |
|
receptor, fibroblast growth factor, type 2 - genetics |
1 |
|
recurrence |
1 |
|
regional blood flow |
1 |
|
reverse transcriptase polymerase chain reaction |
1 |
|
rhabdomyoma |
1 |
|
rhabdomyoma - ultrasonography |
1 |
|
rmrp gene |
1 |
|
rna, messenger - isolation & purification |
1 |
|
sacrococcygeal teratoma |
1 |
|
san diego type |
1 |
|
sequence analysis, dna - methods |
1 |
|
serum alphafetoprotein |
1 |
|
sex determination processes |
1 |
|
skeletal dysplasia |
1 |
|
skull - abnormalities |
1 |
|
smoking - adverse effects |
1 |
|
stai |
1 |
|
stroke volume - physiology |
1 |
|
systole |
1 |
|
tachycardia, supraventricular - diagnosis |
1 |
|
tandem repeat sequences |
1 |
|
teratoma - surgery |
1 |
|
thalassemia |
1 |
|
thalassemia - epidemiology - genetics |
1 |
|
thanatophoric dysplasia |
1 |
|
toes - ultrasonography |
1 |
|
translocation, genetic - genetics |
1 |
|
trisomy - diagnosis |
1 |
|
trisomy - diagnosis - genetics |
1 |
|
trisomy - genetics |
1 |
|
trisomy 18 |
1 |
|
tuberous sclerosis |
1 |
|
tuberous sclerosis - complications |
1 |
|
twins, dichorionic, monozygotic |
1 |
|
twins, monozygotic - genetics |
1 |
|
ultrasonography, prenatal - instrumentation - methods |
1 |
|
ultrasound examination |
1 |
|
uncultured samples |
1 |
|
uniparental disomy |
1 |
|
uniparental disomy (upd) |
1 |
|
ureteral obstruction - congenital - diagnosis - epidemiology |
1 |
|
urethra - abnormalities - ultrasonography |
1 |
|
validity |
1 |
|
vena cava, inferior - embryology - physiology |
1 |
|
vena cava, inferior - physiology |
1 |
|
vocal |
1 |
|
wrist - abnormalities - ultrasonography |
1 |
|
xi vocal |
1 |
|
yqh-acrocentric translocation |
1 |
|
唐氏綜合征 |
1 |
|
染色體異常 |
1 |
|
核型分析 |
1 |
|
特納綜合征 |
1 |
|
產前診斷 |
1 |
