Genotype-phenotype correlations in Noonan syndrome-Reference-Cited by-同舟云学术

Genotype-phenotype correlations in Noonan syndrome

Published:2004-03 Issue:3 Volume:144 Page:368-374
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Zenker Martin,Buheitel Gernot,Rauch Ralf,Koenig Rainer,Bosse Kirstin,Kress Wolfram,Tietze Hans-Ulrich,Doerr Helmuth-Guenther,Hofbeck Michael,Singer Helmut,Reis André,Rauch Anita

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Noonan syndrome;Allanson;J Med Genet,1987

2. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome;Tartaglia;Nat Genet,2001

3. Shp-2 tyrosine phosphatase: signaling one cell or many;Feng;Exp Cell Res,1999

4. Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome;Musante;Eur J Hum Genet,2003

5. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity;Tartaglia;Am J Hum Genet,2002

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