Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes-Reference-Cited by-同舟云学术

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Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes

Published:2004-05-19 Issue:9 Volume:12 Page:718-728
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Mirza Ghazala,Williams Ruth R,Mohammed Shela,Clark Robin,Newbury-Ecob Ruth,Baldinger Shari,Flinter Frances,Ragoussis Jiannis

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201194.pdf

Reference23 articles.

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

2. Kasai O : A case of partial monosomy 6p. Jpn J Hum Genet 1982; 27: 214–215.

3. Guillen-Navarro : A rare de novo microdeletion of distal chromosome 6p: clinical phenotype and molecular cytogenetic characterisation. Am J Hum Genet 1997; 61: A719.

4. Anderlid B-M, Schoumans J, Hallqvist A et al: Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment. Eur J Hum Genet 2003; 11: 89–92.

5. Batanian JR, Grange DK, Fleming R et al: Two unbalanced translocations involving a common 6p25 region in two XY female patients. Clin Genet 2001; 59: 52–57.

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