Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2)-Reference-Cited by-同舟云学术

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Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2)

Published:2003-01 Issue:1 Volume:7 Page:5-12
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Moog Ute,Smeets Eric EJ,van Roozendaal Kees EP,Schoenmakers Sam,Herbergs Jos,Schoonbrood-Lenssen Anneke MJ,Schrander-Stumpel Connie TRM

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference40 articles.

1. Diagnostic criteria for Rett syndrome;Ann Neurol,1988

2. Rett syndrome is caused by mutations in X-linked MeCP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

3. Occurrence of Rett syndrome in boys;Leonard;Child Neurol,2001

4. MeCP2 mutations in children with and without the phenotype of Rett syndrome;Hoffbuhr;Neurology,2001

5. Rett syndrome in a boy with a 47,XXY karotype. confirmed by a rare mutation in the MeCP2 gene;Schwartzman;Neuropediatrics,2001

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