Diversity, parental germline origin, and phenotypic spectrum of de novoHRASmissense changes in Costello syndrome

Author:

Zampino Giuseppe,Pantaleoni Francesca,Carta Claudio,Cobellis Gilda,Vasta Isabella,Neri Cinzia,Pogna Edgar A.,De Feo Emma,Delogu Angelica,Sarkozy Anna,Atzeri Francesca,Selicorni Angelo,Rauen Katherine A.,Cytrynbaum Cheryl S.,Weksberg Rosanna,Dallapiccola Bruno,Ballabio Andrea,Gelb Bruce D.,Neri Giovanni,Tartaglia Marco

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference56 articles.

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2. Germline mutations in HRAS proto-oncogene cause Costello syndrome;Aoki;Nat Genet,2005

3. Ras oncogenes in human cancer: a review;Bos;Cancer Res,1989

4. Parent-of-origin effects in multiple endocrine neoplasia type 2B;Carlson;Am J Hum Genet,1994

5. Germline missense mutations affecting KRAS isoform B are associated with a severe Noonan syndrome phenotype;Carta;Am J Hum Genet,2006

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