Exome sequencing reveals distinct genetic architectures for syndromic and nonsyndromic congenital heart defects

التفاصيل البيبلوغرافية
العنوان: Exome sequencing reveals distinct genetic architectures for syndromic and nonsyndromic congenital heart defects
المؤلفون: Sifrim, Alejandro, Hitz, M, Wilsdon, A, Al Turki, SH, Thienpont, Bernard, McRae, J, Fitzgerald, TW, Singh, T, Swaminathan, GJ, Rajan, D, Prigmore, E, The INTERVAL study, The UK10K Consortium, Competence Network for Congenital Heart Defects, German Register for Congenital Heart Defects, Mital, S, Daubeney, P, Keavney, B, Goodship, J, Abu-Sulaiman, RM, Klaassen, S, Wright, CF, Firth, HV, Barrett, JC, Devriendt, Koenraad, Fitzpatrick, DR, Brook, JD, The Deciphering Developmental Disorders Study, Hurles, ME
سنة النشر: 2016
المجموعة: KU Leuven: Lirias
الوصف: status: published
نوع الوثيقة: conference object
اللغة: English
العلاقة: online abstracts; European Human Genetics Conference 2016 location:Barcelona, Spain date:21-24 May 2016; https://lirias.kuleuven.be/handle/123456789/546369Test; http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=ffd6fece-9aaa-4567-b689-c54cc4f83376&cKey=53289c9c-845f-4813-8112-374dc4539d6c&mKey=724c3001-0be7-4c9f-b314-ddac3db6fc2aTest
الإتاحة: https://lirias.kuleuven.be/handle/123456789/546369Test
http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=ffd6fece-9aaa-4567-b689-c54cc4f83376&cKey=53289c9c-845f-4813-8112-374dc4539d6c&mKey=724c3001-0be7-4c9f-b314-ddac3db6fc2aTest
رقم الانضمام: edsbas.66890CC2
قاعدة البيانات: BASE