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RW

Robert Wilroy

Credentials: ·

Research

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
The American Journal of Human Genetics · 1997 · 312 citations
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor
Cell · 1994 · 259 citations
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions
Case report · The American Journal of Human Genetics · 1993 · 79 citations

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