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Publications by Sau Wai Cheung
Positive Predictive Value Estimates for Cell-Free Noninvasive Prenatal Screening From Data of a Large Referral Genetic Diagnostic Laboratory
American Journal of Obstetrics and Gynecology
Gynecology
Obstetrics
Erratum To: Haploinsufficiency of the E3 Ubiquitin-Protein Ligase Gene TRIP12 Causes Intellectual Disability With or Without Autism Spectrum Disorders, Speech Delay, and Dysmorphic Features
Human Genetics
Genetics
Human Subtelomeric Copy Number Gains Suggest a DNA Replication Mechanism for Formation: Beyond Breakage–fusion–bridge for Telomere Stabilization
Human Genetics
Genetics
Recurrent Deletions and Reciprocal Duplications of 10q11.21q11.23 Including CHAT and SLC18A3 Are Likely Mediated by Complex Low-Copy Repeats
Human Mutation
Genetics
Neurodevelopmental and Neurobehavioral Characteristics in Males and Females With CDKL5 Duplications
European Journal of Human Genetics
Genetics
OEIS Complex Associated With Chromosome 1p36 Deletion: A Case Report and Review
American Journal of Medical Genetics, Part A
Genetics
Xp11.22 Deletions Encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a Cause of Syndromic X-Linked Intellectual Disability
PLoS ONE
Multidisciplinary
A Small Recurrent Deletion Within 15q13.3 Is Associated With a Range of Neurodevelopmental Phenotypes
Nature Genetics
Genetics
Microduplications of 22q11.2 Are Frequently Inherited and Are Associated With Variable Phenotypes
Genetics in Medicine
Medicine
Genetics
Redefined Genomic Architecture in 15q24 Directed by Patient Deletion/Duplication Breakpoint Mapping
Human Genetics
Genetics
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