VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study.

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Bibliographic Details
Title: VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study.
Authors: Calderón JF; Center for Human Genetics, Facultad de Medicina, Clínica Alemana-Universidad del Desarrollo., Puga AR, Guzmán ML, Astete CP, Arriaza M, Aracena M, Aravena T, Sanz P, Repetto GM
Source: Biological research [Biol Res] 2009; Vol. 42 (4), pp. 461-8. Date of Electronic Publication: 2010 Jan 29.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Biomed Central, Ltd Country of Publication: England NLM ID: 9308271 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 0717-6287 (Electronic) Linking ISSN: 07169760 NLM ISO Abbreviation: Biol Res Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:0717-6287
DOI:/S0716-97602009000400007