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  11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features.

Kariminejad, A., Kariminejad, R., Tzschach, A., Najafi, H., Ahmed, A., Ullmann, R., et al. (2010). 11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features. American Journal of Medical Genetics. Part A., 152A(10), 2651-2655. doi:10.1002/ajmg.a.33623.

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Genre: Journal Article
Alternative Title : Am. J. Med. Genet. A

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33623_ftp.pdf (Any fulltext), 120KB
 
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 Creators:
Kariminejad, Ariana, Author
Kariminejad, Roxana, Author
Tzschach, Andreas1, Author           
Najafi, Hamid, Author
Ahmed, Alischo2, Author           
Ullmann, Reinhard2, Author           
Ropers, Hans-Hilger1, Author           
Kariminejad, Mohamad Hasan, Author
Affiliations:
1Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433549              
2Molecular Cytogenetics (Reinhard Ullmann), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479645              

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Language(s): eng - English
 Dates: 2010-08-26
 Publication Status: Issued
 Pages: -
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Title: American Journal of Medical Genetics. Part A.
  Alternative Title : Am. J. Med. Genet. A
Source Genre: Journal
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Pages: - Volume / Issue: 152A (10) Sequence Number: - Start / End Page: 2651 - 2655 Identifier: ISSN: 1552-4825