A.H.M. Mahbubul Huq

A unique mutation in the vitamin D receptor gene in three Japanese patients with vitamin D-dependent rickets type II: utility of single-strand conformation polymorphism analysis for heterozygous carrier detection.

Takahiko Saijo, Masaaki Ito, Eiji Takeda et al. · PubMed · 1991 · 196 citations

Association of Reelin gene polymorphisms with autism

Fatema Serajee, Hailang Zhong, A.H.M. Mahbubul Huq · Genomics · 2005 · 124 citations

Developmental Biology, Syndromic Autism, Genetics +6

Association of tryptophan 2,3 dioxygenase gene polymorphism with autism

Rafiqun Nabi, Fatema Serajee, Diane C. Chugani et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2003 · 76 citations

X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death

A.H.M. Mahbubul Huq, Rhonda S. Lovell, C N Ou et al. · Human Molecular Genetics · 1997 · 65 citations · Full text

Metabolic Disorder, Genetics, Glycerol Kinase Deficiency +23

Abnormal Language Pathway in Children With Angelman Syndrome

Benjamin J. Wilson, Senthil K. Sundaram, A.H.M. Mahbubul Huq et al. · Pediatric Neurology · 2011 · 61 citations

Child Language, Language Acquisition, Psycholinguistics +3