Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management-Reference-Cited by-同舟云学术

Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management

Published:2007-02-13 Issue:7 Volume:44 Page:494-497
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Cornish K,Bramble D

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2002.tb00312.x/fullpdf

Reference38 articles.

1. Trois cas de deletion partielle du bras court d'un chromosome 5;Lejeune;Comptes Rendusde l Academie des Sciences. Serie 111, Sciences de la Vie Paris,1963

2. Neurological abnormalities in the ‘cri-du-chat’ syndrome;Colover;Journal of Neurology, Neurosurgery and Psychiatry,1972

3. The cri-du-chat syndrome;Gordon;Developmental Medicine & Child Neurology,1965

4. Facial appearance in cri du chat syndrome;Gordon;Developmental Medicine & Child Neurology,1968

5. Pseudohypoparathyroidism associated with cri-du-chat syndrome;Kee;Medical Journal of Austria,1976

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