Rethinking the fate of males with mutations in the gene that causes Rett syndrome-Reference-Cited by-同舟云学术

Rethinking the fate of males with mutations in the gene that causes Rett syndrome

Published:2001-12 Issue: Volume:23 Page:S144-S146
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Schanen Carolyn

Publisher

Elsevier BV

Subject

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

Reference19 articles.

1. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases;Hagberg;Ann Neurol,1983

2. The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation;Comings;Am J Med Genet Suppl,1986

3. Rett syndrome – observational study of 33 families;Murphy;Am J Med Genet Suppl,1986

4. High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders;Thomas;Am J Hum Genet,1996

5. Neonatal encephalopathy in two boys in families with recurrent Rett syndrome;Schanen;J Child Neurol,1998

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