Stephen T.S. Lam

NSD1 mutations generate a genome-wide DNA methylation signature

Sanaa Choufani, Cheryl Cytrynbaum, Brian Hon‐Yin Chung et al. · Nature Communications · 2015 · 206 citations · Full text

Novel<i>FOXF1</i>Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

Partha Sen, Yaping Yang, C. Navarro et al. · Human Mutation · 2013 · 114 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +15

Cytogenetic analysis of patients with primary and secondary amenorrhoea in Hong Kong: retrospective study.

Marcy Zenobi‐Wong, Stephen T.S. Lam · PubMed · 2005 · 31 citations

Fertility, Cytogenetics, Genetics +20

Trinucleotide CGG repeat in theFMR1 gene in Chinese mentally retarded patients

Chi‐Pui Pang, Priscilla M.K. Poon, Qian L. Chen et al. · American Journal of Medical Genetics · 1999 · 26 citations

High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardation

Albert C.F. Lam, Stephen T.S. Lam, Kent Lai et al. · Clinical Biochemistry · 2006 · 23 citations

Neuropsychology, Subtelomeric Aberration, Ophthalmology +8