Using Affected Sib-Pairs to Uncover Rare Disease Variants

Perdry, Herve; Mueller-Myhsok, Bertram; Clerget-Darpoux, Francoise

doi:10.1159/000346788

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Using Affected Sib-Pairs to Uncover Rare Disease Variants

Perdry, H., Mueller-Myhsok, B., & Clerget-Darpoux, F. (2013). Using Affected Sib-Pairs to Uncover Rare Disease Variants. HUMAN HEREDITY, 74(3-4), 129-141. doi:10.1159/000346788.

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Datensatz-Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-CD34-9 Versions-Permalink: https://hdl.handle.net/11858/00-001M-0000-0019-0920-3

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Urheber:
Perdry, Herve¹, Autor
Mueller-Myhsok, Bertram², Autor
Clerget-Darpoux, Francoise¹, Autor

Affiliations:
1external, ou_persistent22
2AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607154