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  Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome)

Hoffer, J. L., Fryssira, H., Konstantinidou, A., Ropers, H.-H., & Tzschach, A. (2013). Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical Genetics: an international journal of genetics in medicine, 83(1), 92-95. doi:10.1111/j.1399-0004.2012.01880.x.

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© 2012 John Wiley & Sons A/S. Published by Blackwell Publishing Ltd
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 Creators:
Hoffer, J. L., Author
Fryssira, H., Author
Konstantinidou, A., Author
Ropers, H.-H.1, Author              
Tzschach, A.1, 2, Author              
Affiliations:
1Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, Berlin, Germany, ou_1433549              
2Institute of Human Genetics, University of Tübingen, Tübingen, Germany, ou_persistent22              

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Language(s): eng - English
 Dates: 2012-04-092013-01
 Publication Status: Published in print
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1111/j.1399-0004.2012.01880.x
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Title: Clinical Genetics: an international journal of genetics in medicine
  Other : Clin. Genet.
Source Genre: Journal
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Publ. Info: Copenhagen : Munksgaard
Pages: - Volume / Issue: 83 (1) Sequence Number: - Start / End Page: 92 - 95 Identifier: ISSN: 0009-9163
CoNE: https://pure.mpg.de/cone/journals/resource/954925391292