Multiple endocrine neoplasia type 2RETprotooncogene database: Repository of MEN2-associatedRETsequence variation and reference for genotype/phenotype correlations-Reference-Cited by-同舟云学术

Multiple endocrine neoplasia type 2RETprotooncogene database: Repository of MEN2-associatedRETsequence variation and reference for genotype/phenotype correlations

Published:2009-04 Issue:4 Volume:30 Page:548-556
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Margraf Rebecca L.,Crockett David K.,Krautscheid Patti M.F.,Seamons Ryan,Calderon Fernanda R.O.,Wittwer Carl T.,Mao Rong

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference110 articles.

1. The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case;Aiello;Surgery,2005

2. Genetic testing in pheochromocytoma or functional paraganglioma;Amar;J Clin Oncol,2005

3. Hirschsprung disease, associated syndromes and genetics: a review;Amiel;J Med Genet,2008

4. Biological effects of the dual phenotypic Janus mutation of ret cosegregating with both multiple endocrine neoplasia type 2 and Hirschsprung's disease;Arighi;Mol Endocrinol,2004

5. A RET mutation with decreased penetrance in the family of a patient with a ��sporadic�� pheochromocytoma;Arum;Endocrine,2005

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