Results 1 to 20 of 24
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TypeTitleAuthor(s)YearViews
A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counselingLuk, HM; Wong, VCH; Lo, IFM; Chan, YK; Lau, ETK; Kan, SYA; Tang, MHY; Tang, WF; She, WMK; Chu, WY; Sin, WK; Chung, BHY201422
 
Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong KongKan, SYA; Lau, ETK; Tang, WF; Chan, SSY; Ding, SCK; Chan, YK; Lee, CP; Hui, PW; Chung, BHY; Leung, KY; Ma, WLT; Leung, WC; Tang, MHY201428
 
Integration of chromosomal microarray into paediatric clinical care in Hong KongTao, QV; Chu, WY; Chan, YK; Lau, ETK; Mok, TKG; Tso, WYW; Liu, APY; Kan, SYA; Tang, MHY; Lau, YL; Chung, BHY201320
 
Evidence of spread of X chromosome inactivation on chromosome 15 in a girl with an unbalanced t(X;15) transolcationYEUNG, KS; Chee, WYY; Luk, HM; Tang, MHY; Lau, ETK; Shuen, YA; Lo, IFM; Chan, YK; Chung, BHY201328
 
Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of LiteratureLiu, APY; Tang, WF; Lau, ETK; Chan, YK; Kan, SYA; Wong, KY; Tso, WYW; Jalal, K; Lee, SL; Chau, CSK; Chung, BHY2013166
 
Prenatal Diagnosis of Agenesis of the Corpus Callosum and Cerebellar Vermian Hypoplasia Associated with a Microdeletion on Chromosome 1p32: Decision Minor revisionTang, MHY; Lau, ETK; Tan, TY; Chung, BHY; Shek, NWM201344
 
Integration of chromosomal microarray into paediatric clinical care in Hong KongTao, QV; She, W; Chu, WY; Tso, WYW; Chan, KY; Lau, ETK; Kan, SYA; Tang, MHY; Lau, YL; Chung, BHY201339
 
22q11.2 deletion syndrome in adult Chinese patient with conotruncal anomalies: Dysmorphisms, clinical features and under-diagnosisLiu, APY; Chow, PC; Lee, PPW; Mok, TKG; Tang, WF; Lau, ETK; Lam, STS; Chan, KY; Kan, SYA; Chau, AKT; Cheung, YF; Lau, YL; Chung, BHY201336
 
Alport's syndrome: case of a giant esophageal tumorTsang, JS; Tong, DKH; Chung, BHY; Tang, MHY; Lau, ETK; Chan, GCF; Law, SYK2013105
 
22q11.2 deletion syndrome in adult Chinese patients with conotruncal anomalies: dysmorphisms, clinical features and under-diagnosisLiu, APY; Chow, PC; Lee, PPW; Mok, TKG; Tang, WF; Lau, ETK; Lam, STS; Chan, YK; Kan, SYA; Chau, AKT; Cheung, YF; Lau, YL; Chung, BHY201333
 
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition careChung, B; Chow, P; Liu, A; Lee, P; Wong, V; Chan, K; Tang, M; Lun, KS; Lau, ETK; Cheung, YF; Chau, KT; Lau, YL201333
 
Update on Basic Science or Lab Technique - Array CGH for Prenatal DiagnosisLau, ETK201240
 
Disclosing results of autism genomic testing-systematic review and applying its results to clinical practiceChung, B; Cheuk, DKL; Tang, M; Lau, ETK; Chan, YK; Lau, YL201296
 
Findings on Prenatal aCGH evaluationLau, ETK201138
 
Molecular Cytogenetics and Application-1Lau, ETK201143
 
Evaluation of aCGH for Prenatal DiagnosisLau, ETK201142
 
Principle and Diagnostic pitfall of PCR and FISHLau, ETK201144
 
Prenatal Diagnostic Service – PresentLau, ETK201140
 
Evaluation of aCGH for Prenatal Diagnosis.Lau, ETK201140
 
Maternal serum anti-Mullerian hormone level is not superior to chronological age in predicting down syndrome pregnanciesLi, HWR; Hui, PW; Tang, MHY; Lau, ETK; Yeung, WSB; Ho, PC; Ng, EHY2010181
 
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