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Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Soemedi, Rachel; Wilson, Ian J; Bentham, Jamie; Darlay, Rebecca; Töpf, Ana; Zelenika, Diana; Cosgrove, Catherine; Setchfield, Kerry; Thornborough, Chris; Granados-Riveron, Javier; Blue, Gillian M; Breckpot, Jeroen; Hellens, Stephen; Zwolinkski, Simon; Glen, Elise; Mamasoula, Chrysovalanto; Rahman, Thahira J; Hall, Darroch; Rauch, Anita; Devriendt, Koenraad; Gewillig, Marc; O' Sullivan, John; Winlaw, David S; Bu'Lock, Frances; Brook, J David; Bhattacharya, Shoumo; Lathrop, Mark; Santibanez-Koref, Mauro; Cordell, Heather J; Goodship, Judith A; Keavney, Bernard D.
Affiliation
  • Soemedi R; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
Am J Hum Genet ; 91(3): 489-501, 2012 Sep 07.
Article in En | MEDLINE | ID: mdl-22939634
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Deletion / DNA Copy Number Variations / Heart Defects, Congenital Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2012 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Deletion / DNA Copy Number Variations / Heart Defects, Congenital Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2012 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos