Showing results 29 to 34 of 34
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Title | Author(s) | Issue Date | |
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Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics | 2014 | ||
Update on Basic Science or Lab Technique: Array CGH for Prenatal Diagnosis Proceeding/Conference:Conference in Department of Obstetrics and Gynaecology, The University of Hong Kong | 2012 | ||
Use of chromosomal microarray in Hong Kong patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016 | 2016 | ||
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 |