Whole exome sequencing for prenatal diagnosis of CHARGE syndrome: a case report
Author(s) -
Irene WY Lok,
CW Kong,
Anita SY Kan,
KS Yeung,
Mullin HC Yu,
Brian HY Chung,
William WK To
Publication year - 2019
Publication title -
hong kong journal of gynaecology obstetrics and midwifery
Language(s) - English
Resource type - Journals
eISSN - 2225-904X
pISSN - 1608-9367
DOI - 10.12809/hkjgom.19.2.06
Subject(s) - exome sequencing , charge syndrome , exome , medicine , prenatal diagnosis , computational biology , genetics , biology , mutation , pregnancy , fetus , gene
Irene WY LOK1 MBChB, MRCOG, FHKAM (O&G) CW KONG1 MBChB, MSc in Medical Genetics, MRCOG, FHKAM (O&G), Cert HKCOG (MFM) Anita SY KAN2,3 MBBS, MPH(HK), MRCOG, FHKCOG, FHKAM (O&G) KS YEUNG4 PhD Mullin HC YU4 MSc Brian HY CHUNG4 MBBS(Hons, HKU), MSc(Genomics and Bioinformatics, CUHK), MD(HKU), DCH(Ireland), MRCPCH (UK), FHKAM(Paediatrics), FRCPCH(UK), FCCMG(Clinical Genetics, Canada) William WK TO1 MBBS, MPH, M Phil, MD, Dip med, FHKAM (O&G), Cert HKCOG (MFM) 1 Department of Obstetrics and Gynaecology, United Christian Hospital 2 Department of Obstetrics and Gynaecology, Queen Mary Hospital 3 Prenatal Diagnostic Laboratory, Tsan Yuk Hospital 4 Department of Paediatrics and Adolescent Medicine, The University of Hong Kong
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