Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment-Reference-Cited by-同舟云学术

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Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment

Published:2003-01 Issue:1 Volume:11 Page:89-92
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Anderlid Britt-Marie,Schoumans Jacqueline,Hallqvist Åsa,Ståhl Ylva,Wallin Agneta,Blennow Elisabeth,Nordenskjöld Magnus

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200907.pdf

Reference19 articles.

1. Palmer CG, Bader P & Slovak ML et al: Partial deletion of chromosome 6p: delineation of the syndrome. Am J Med Genet 1991; 39: 155–160.

2. Davies AF, Olavesen MG, Stephens RJ, Comings DE & Pettenati MJ : A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome. Hum Genet 1996; 98: 454–459.

3. Davies AF, Mirza G & Sekhon G et al: Delineation of two distinct 6p deletion syndromes. Hum Genet 1999; 104: 64–72.

4. Knight SJ, Regan R & Nicod A et al: Subtle chromosomal rearrangements in children with unexplained mental retardation. Lancet 1999; 354: 1676–1681.

5. Law CJ, Fisher AM & Temple IK : Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports. J Med Genet 1998; 35: 685–689.

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