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

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Language(s): eng - English
 Dates: 2013-04
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000317089300004
DOI: 10.1038/ejhg.2012.198
 Degree: -

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Title: EUROPEAN JOURNAL OF HUMAN GENETICS
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 21 (4) Sequence Number: - Start / End Page: 367 - 372 Identifier: ISSN: 1018-4813