X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies-Reference-Cited by-同舟云学术

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X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies

Published:2008-06-28 Issue:3 Volume:52 Page:155-161
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Claes Stephan,Devriendt Koenraad,D'Adamo Patrizia,Meireleire Jan,Raeymaekers Peter,Toniolo Daniela,Cassiman Jean-Jacques,Fryns Jean-Pierre

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02536.x/fullpdf

Reference23 articles.

1. Transcriptional organization of a 450-kb region on the human X chromosome in Xq28;Bione;PNAS,1993

2. Hereditary cerebral palsy: a preliminary report;Blumel;J Pediatr,1957

3. X-linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus;Bonneau;J Med Genet,1993

4. HSAS and SPG1 result from a donor splice site mutation in the L1CAM gene in a Venezuelan pedigree;Claes;Hum Mutat,1997

5. X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq2S;Fryns;J Med Genet,1991

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4. X-Linked Mental Retardation (XLMR): From Clinical Conditions to Cloned Genes;Critical Reviews in Clinical Laboratory Sciences;2004-01

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