G. Meyers

发表

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

G. Buck, B. Wolf, J. Hymes, 1997, Pediatric Research.

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

I. Munro, E. Jabs, S. Orlow, 1995, Nature Genetics.

High Prevalence of GB Virus C in Brazil and Molecular Evidence for Intrafamilial Transmission

P. Zanotto, G. Buck, F. Carrilho, 1999, Journal of Clinical Microbiology.

Structure of the human biotinidase gene

G. Buck, Heather Knight, B. Wolf, 1998, Mammalian Genome.

Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses

A. Pandya, G. Buck, P. Melone, 1998, Prenatal diagnosis.

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.

E. Jabs, A. F. Scott, J. Graham, 1996, American journal of human genetics.

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

E. Jabs, S. Orlow, C. Theda, 1995, Human molecular genetics.

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

M. Eccles, E. Jabs, A. F. Scott, 1994, Nature Genetics.

Transfusion-transmitted virus (TTV) in Brazil. Preliminary report.

G. Buck, M. Soares, J. Pinho, 1998, Revista do Instituto de Medicina Tropical de Sao Paulo.

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

E. Jabs, C. Theda, C. Dufresne, 1995, American journal of human genetics.

Craniosynostosis and skeletal dysplasias: fibroblast growth factor receptor defects.

E. Jabs, A. Lewanda, G. Meyers, 1996, Proceedings of the Association of American Physicians.