Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34378/fullpdf
Reference15 articles.
1. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32);Abuelo;J Med Genet,1982
2. Intermediate interstitial deletion of chromosome 7q detected by first-trimester Down's syndrome screening;Cheong;Fetal Diagn Ther,2008
3. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia;Feuk;Am J Hum Genet,2006
4. Two cases with different deletions of the long arm of chromosome 7;Klep-de Pater;J Med Genet,1979
5. A forkhead-domain gene is mutated in a severe speech and language disorder;Lai;Nature,2001
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