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Browsing by Subject x chromosome
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Showing results 15 to 29 of 29
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Title
Author(s)
Issue Date
Intragenic dinucleotide repeats in factor VIII gene for the diagnosis of haemophilia A
Journal:
British Journal of Haematology
Yip, B
Chan, V
Chan, TK
1994
Isolation of full-length cDNA and chromosomal localization of human NF- κB modulator NEMO to Xq28
Journal:
Journal of Biomedical Science
Jin, DY
Jeang, KT
1999
Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis
Journal:
American Journal of Human Genetics
Musarella, MA
Burghes, A
AnsonCartwright, L
Mahtani, MM
Argonza, R
Tsui, LC
Worton, R
1988
Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLE
Journal:
Arthritis Research & Therapy
ZHANG, H
ZHANG, Y
Wang, Y
Shen, JJ
Yang, J
Lau, YL
Yang, W
2018
Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A
Journal:
British Journal of Haematology
Chan, V
Tong, TMF
Chan, TPT
Tang, M
Wan, CW
Chan, FY
Chu, YC
Chan, TK
1989
The murine Xe169 gene escapes X-inactivation like its human homologue
Journal:
Nature Genetics
Wu, J
Salido, EC
Yen, PH
Mohandas, TK
Heng, HHQ
Tsui, LC
Park, J
Chapman, VM
Shapiro, LJ
1994
Ovarian mature cystic teratoma with malignant transformation: An interphase cytogenetic study
Journal:
International Journal of Gynecological Pathology
Shen, DH
Khoo, US
Xue, WC
Cheung, ANY
1998
Prenatal quantitation of number of X-chromosomes by slot blot hybridization and autoradiography
Journal:
International Journal of Gynecology and Obstetrics
Chan, FY
Chan, V
Chan, TK
1993
Production of anti-phosphorylcholine antibodies of the T15 idiotype in CBA/N xid mice: Investigation of the defect using a T15 immunoglobulin transgene
Journal:
Molecular Immunology
Lim, PL
Chan, STH
Leung, DTM
Ng, SSM
Loh, TT
1994
Schizophrenia and the androgen receptor gene: Report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families
Journal:
American Journal of Medical Genetics - Neuropsychiatric Genetics
Arranz, M
Sharma, T
Sham, P
Kerwin, R
Nanko, S
Owen, M
Gill, M
Collier, D
1995
Statistical analysis in genetic imprinting on the X chromosome and DNA forensics
Yu, Kexin
俞可歆
Advisor(s):
Fung, TWK
2017
Statistical analysis of parent-of-origin effects on the X chromosome and DNA methylation on age prediction
Lau, Pui Yin
劉沛彥
Advisor(s):
Fung, TWK
2019
Two Powerful Tests for Parent-of-Origin Effects at Quantitative Trait Loci on the X Chromosome
Journal:
Human Heredity
LAU, PY
Yeung, KF
Zhou, JY
Fung, WK
2019
X-CGDbase: A database of X-CGD-causing mutations
Journal:
Immunology Today
Roosl, D
Curnutte, JT
Hossle, JP
Lau, YL
Ariga, T
Nunoi, H
Dinauer, MC
Gahr, M
Segal, AW
Newburger, PE
Giacca, M
Keep, NH
Van Zwieten, R
1996
X-linked polymorphism of hypoxanthine phosphoribosyl transferase gene (HPRT) in Chinese females [2]
Journal:
Cancer Genetics and Cytogenetics
Chan, LC
Tse, E
Pittaluga, S
1992