6p25 Interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder-Reference-Cited by-同舟云学术

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6p25 Interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder

Published:2013-05 Issue:3 Volume:17 Page:225-231
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Bozza Margherita,Bernardini Laura,Novelli Antonio,Brovedani Paola,Moretti Elena,Canapicchi Raffaello,Doccini Viola,Filippi Tiziana,Battaglia Agatino

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference33 articles.

1. Partial deletion of chromosome 6p: autopsy findings in a premature infant and review of the literature;Alashari;Pediatr Pathol Lab Med,1995

2. FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation;Aldinger;Nat Genet,2009

3. Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment;Anderlid;Eur J Hum Genet,2003

4. A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia;Bedoyan;Am J Med Genet A,2011

5. Mild developmental delay in terminal chromosome 6p deletion;Chen;Am J Med Genet,2004

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