Binquan Huang

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

Susan L. Christian, Wendy P. Robinson, Binquan Huang et al. · PubMed · 1995 · 189 citations

Life Sciences, Molecular Genetics, Molecular Medicine +7

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

Binquan Huang, John A. Crolla, Susan L. Christian et al. · Human Genetics · 1996 · 115 citations

Life Sciences, Genetics, Molecular Genetics +9

Genomic sequence of the DAX1 gene: an orphan nuclear receptor responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.

Wenya Guo, Thomas P. Burris, Y H Zhang et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 82 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Glycerol kinase deficiency: Evidence for complexity in a single gene disorder

Katrina M. Dipple, Y.-H. Zhang, Binquan Huang et al. · Human Genetics · 2001 · 74 citations

Life Sciences, Genetics, Molecular Genetics +11

AluY insertion (IVS4-52ins316alu) in the glycerol kinase gene from an individual with benign glycerol kinase deficiency

Y.-H. Zhang, Katrina M. Dipple, Éric Vilain et al. · Human Mutation · 2000 · 41 citations

Life Sciences, Genetics, Molecular Genetics +15