Bannayan–Riley–Ruvalcaba syndrome with reactive nodular lymphoid hyperplasia and autism and a PTEN mutation-Reference-Cited by-同舟云学术

Bannayan–Riley–Ruvalcaba syndrome with reactive nodular lymphoid hyperplasia and autism and a PTEN mutation

Published:2006 Issue:18 Volume:140A Page:1965-1969
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Boccone Loredana,Dessì Valentina,Zappu Antonietta,Piga Silvia,Piludu Maria Bonaria,Rais Marco,Massidda Carlo,De Virgiliis Stefano,Cao Antonio,Loudianos Georgios

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

2. A new lipid storage myopathy observed in individuals with the Ruvalcaba-Myhre-Smith syndrome

3. NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes

4. Will the real Cowden syndrome please stand up: revised diagnostic criteria

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