Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families 
with unknown genetic defects

Arelin, Maria; Schulze, Bernt; Mueller-Myhsok, Bertram; Horn, Denise; Diers, Alexander; Uhlenberg, Birgit; Nuernberg, Peter; Nuernberg, Gudrun; Becker, Christian; Mundlos, Stefan; Lindner, Tom H.; Sperling, Karl; Hoffmann, Katrin

doi:10.1038/ejhg.2012.198

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Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects

Arelin, M., Schulze, B., Mueller-Myhsok, B., Horn, D., Diers, A., Uhlenberg, B., et al. (2013). Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects. EUROPEAN JOURNAL OF HUMAN GENETICS, 21(4), 367-372. doi:10.1038/ejhg.2012.198.

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Datensatz-Permalink: https://hdl.handle.net/11858/00-001M-0000-0015-1109-3 Versions-Permalink: https://hdl.handle.net/11858/00-001M-0000-0018-5AB3-D

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Urheber:
Arelin, Maria¹, Autor
Schulze, Bernt¹, Autor
Mueller-Myhsok, Bertram², Autor
Horn, Denise¹, Autor
Diers, Alexander¹, Autor
Uhlenberg, Birgit¹, Autor
Nuernberg, Peter¹, Autor
Nuernberg, Gudrun¹, Autor
Becker, Christian³, Autor
Mundlos, Stefan⁴, Autor
Lindner, Tom H.¹, Autor
Sperling, Karl¹, Autor
Hoffmann, Katrin⁴, Autor

Affiliations:
1external, ou_persistent22
2AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607154
3External Organizations, ou_persistent22
4Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557