Meyers GA - Search Results

1

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

Meyers GA, Orlow SJ, Munro IR, Przylepa KA, Jabs EW. Meyers GA, et al. Nat Genet. 1995 Dec;11(4):462-4. doi: 10.1038/ng1295-462. Nat Genet. 1995. PMID: 7493034

2

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

Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eccles M, Mao JI, Charnas LR, Jackson CE, Jaye M. Jabs EW, et al. Nat Genet. 1994 Nov;8(3):275-9. doi: 10.1038/ng1194-275. Nat Genet. 1994. PMID: 7874170

3

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Park WJ, Theda C, Maestri NE, Meyers GA, Fryburg JS, Dufresne C, Cohen MM Jr, Jabs EW. Park WJ, et al. Among authors: meyers ga. Am J Hum Genet. 1995 Aug;57(2):321-8. Am J Hum Genet. 1995. PMID: 7668257 Free PMC article.

4

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

Park WJ, Meyers GA, Li X, Theda C, Day D, Orlow SJ, Jones MC, Jabs EW. Park WJ, et al. Among authors: meyers ga. Hum Mol Genet. 1995 Jul;4(7):1229-33. doi: 10.1093/hmg/4.7.1229. Hum Mol Genet. 1995. PMID: 8528214

5

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.

Meyers GA, Day D, Goldberg R, Daentl DL, Przylepa KA, Abrams LJ, Graham JM Jr, Feingold M, Moeschler JB, Rawnsley E, Scott AF, Jabs EW. Meyers GA, et al. Am J Hum Genet. 1996 Mar;58(3):491-8. Am J Hum Genet. 1996. PMID: 8644708 Free PMC article.

6

Craniosynostosis and skeletal dysplasias: fibroblast growth factor receptor defects.

Lewanda AF, Meyers GA, Jabs EW. Lewanda AF, et al. Among authors: meyers ga. Proc Assoc Am Physicians. 1996 Jan;108(1):19-24. Proc Assoc Am Physicians. 1996. PMID: 8834060 Review. No abstract available.

7

Structure of the human biotinidase gene.

Knight HC, Reynolds TR, Meyers GA, Pomponio RJ, Buck GA, Wolf B. Knight HC, et al. Among authors: meyers ga. Mamm Genome. 1998 Apr;9(4):327-30. doi: 10.1007/s003359900760. Mamm Genome. 1998. PMID: 9530634

8

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

Pomponio RJ, Hymes J, Pandya A, Landa B, Melone P, Javaheri R, Mardach R, Morton SW, Meyers GA, Reynolds T, Buck G, Nance WE, Wolf B. Pomponio RJ, et al. Among authors: meyers ga. Prenat Diagn. 1998 Feb;18(2):117-22. Prenat Diagn. 1998. PMID: 9516011

9

High prevalence of GB virus C in Brazil and molecular evidence for intrafamilial transmission.

Pinho JR, Zanotto PM, Ferreira JL, Sumita LM, Carrilho FJ, da Silva LC, Capacci ML, Silva AO, Guz B, Gonçales FL Jr, Gonçales NS, Buck GA, Meyers GA, Bernardini AP. Pinho JR, et al. Among authors: meyers ga. J Clin Microbiol. 1999 May;37(5):1634-7. doi: 10.1128/JCM.37.5.1634-1637.1999. J Clin Microbiol. 1999. PMID: 10203545 Free PMC article.

10

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

Pinho JR, Takahashi DA, Fava AL, Gonçales NS, Carrilho FJ, Stucchi RS, Gonçales Júnior FL, Da Silva LC, Soares MC, Bensabath G, Buck GA, Meyers GA, Bernardini AP. Pinho JR, et al. Among authors: meyers ga. Rev Inst Med Trop Sao Paulo. 1998 Sep-Oct;40(5):335-6. doi: 10.1590/s0036-46651998000500015. Rev Inst Med Trop Sao Paulo. 1998. PMID: 10030083 English, Portuguese.

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