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

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Mueller-Myhsok, Bertram
AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society;

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Mundlos, Stefan
Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Hoffmann, Katrin
Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Arelin, M., Schulze, B., Mueller-Myhsok, B., Horn, D., Diers, A., Uhlenberg, B., Nuernberg, P., Nuernberg, G., Becker, C., Mundlos, S., Lindner, T. H., Sperling, K., & Hoffmann, K. (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.

引用: https://hdl.handle.net/11858/00-001M-0000-0015-1109-3

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