Chromosome deletion 17pl 1.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation-Reference-Cited by-同舟云学术

Chromosome deletion 17pl 1.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation

Published:2008-06-28 Issue:1 Volume:51 Page:71-74
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Behjati F.,Mullarkey M.,Bergbaum A.,Berry A. C.,Docherty Z.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02420.x/fullpdf

Reference9 articles.

1. Where have all the fragile X boys gone;Barnicoat;Dev Med Child Neurol,1993

2. Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2p11.2) (Smith-Magenis syndrome);Colley;J Paediatr Child Health,1990

3. Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17) (p11.2);Greenberg;Am J Hum Genet,1991

4. Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del(17) (pll.2pll.2);Kondo;Am J Med Genet,1991

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