Concepedia

Binquan Huang

BH

6

Publications

541

Citations

6

H-Index

1995

Active since

Affiliations

National Institutes of Health(Current)

Mattel Children's Hospital

University of California, Los Angeles

Binquan Huang is an author at National Institutes of Health specializing in genetics, medicine, and molecular genetics.

ORCID

Top concepts

Publications per year

1995–2001

6

Publications

6

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

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

, , +10

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

, , +21

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

Katrina M. Dipple, Y.-H. Zhang, Binquan Huang et al. · Human Genetics · 2001 · 73 citations

, , +7

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

, , +13

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