TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg201216.pdf
Reference53 articles.
1. Holt M, Oram S : Familial heart disease with skeletal malformations. Br Heart J 1960; 22: 236–242.
2. Hurst JA, Hall CM, Baraitser M : The Holt-Oram syndrome. J Med Genet 1991; 28: 406–410.
3. Allanson JE, Newbury-Ecob RA : Holt-Oram syndrome: is there a ‘face’? Am J Med Genet 2003; 118A: 314–318.
4. Smith AT, Sack Jr GH, Taylor GJ : Holt-Oram syndrome. J Pediatr 1979; 95: 538–543.
5. Newbury-Ecob RA, Leanage R, Raeburn JA, Young ID : Holt-Oram syndrome: a clinical genetic study. J Med Genet 1996; 33: 300–307.
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