ALK2 mutation in a patient with Down's syndrome and a congenital heart defect-Reference-Cited by-同舟云学术

ALK2 mutation in a patient with Down's syndrome and a congenital heart defect

Published:2011-01-19 Issue:4 Volume:19 Page:389-393
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Joziasse Irene C,Smith Kelly A,Chocron Sonja,van Dinther Maarten,Guryev Victor,van de Smagt Jasper J,Cuppen Edwin,ten Dijke Peter,Mulder Barbara JM,Maslen Cheryl L,Reshey Benjamin,Doevendans Pieter A,Bakkers Jeroen

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2010224.pdf

Reference25 articles.

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3. Owens JR, Harris F, Walker S, McAllister E, West L : The incidence of Down's syndrome over a 19-year period with special reference to maternal age. J Med Genet 1983; 20: 90–93.

4. Korenberg JR, Chen XN, Schipper R et al: Down syndrome phenotypes: the consequences of chromosomal imbalance. Proc Natl Acad Sci USA 1994; 91: 4997–5001.

5. Wiseman FK, Alford KA, Tybulewicz VL, Fisher EM : Down syndrome--recent progress and future prospects. Hum Mol Genet 2009; 18: R75–R83.

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