Showing results 10 to 15 of 15
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Title | Author(s) | Issue Date | |
---|---|---|---|
A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling Journal:European Journal of Medical Genetics | 28-Jan-2014 | ||
Redefining prognostication of de novo cytogenetically normal acute myeloid leukemia in young adults Journal:Blood Cancer Journal | 2020 | ||
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics | 2014 | ||
2017 | |||
Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016 | 2016 | ||
2014 |