Syndromic patent ductus arteriosus: Evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder-Reference-Cited by-同舟云学术

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Syndromic patent ductus arteriosus: Evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder

Published:2005-01-31 Issue:8 Volume:102 Page:2975-2979
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Mani A.,Radhakrishnan J.,Farhi A.,Carew K. S.,Warnes C. A.,Nelson-Williams C.,Day R. W.,Pober B.,State M. W.,Lifton R. P.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference39 articles.

1. Congenital Heart Disease in 56,109 Births Incidence and Natural History

2. Congenital heart disease in a cohort of 19,502 births with long-term follow-up

3. CONGENITAL HEART DISEASE: PREVALENCE AT LIVEBIRTH

4. Histopathology of the arterial duct (ductus arteriosus) with and without treatment with prostaglandin E1

5. Histologic studies on normal and persistent ductus arteriosus in the dog

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