Gregory A. Meyers

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans

Gregory A. Meyers, Seth J. Orlow, Ian R. Munro et al. · Nature Genetics · 1995 · 392 citations

Fibrosis, Mendelian Disorder, Genetic Disorder +11

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Woojin Park, Christiane Theda, Nancy E. Maestri et al. · PubMed · 1995 · 262 citations

Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability

W.-J. Park, Gregory A. Meyers, Xun Li et al. · Human Molecular Genetics · 1995 · 173 citations

FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing.

Gregory A. Meyers, David A. Day, Rosalie Goldberg et al. · PubMed · 1996 · 170 citations

Mutations in the Human Biotinidase Gene That Cause Profound Biotinidase Deficiency in Symptomatic Children: Molecular, Biochemical, and Clinical Analysis

Robert J. Pomponio, Jeanne Hymes, Thomas Reynolds et al. · Pediatric Research · 1997 · 83 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8