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11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features.
Authors: Kariminejad, Ariana; Kariminejad, Roxana; Tzschach, Andreas; Najafi, Hamid; Ahmed, Alischo; Ullmann, Reinhard; Ropers, Hans-Hilger; Kariminejad, Mohamad Hasan
Date of Publication (YYYY-MM-DD): 2010-08-26
Title of Journal: American Journal of Medical Genetics. Part A.
Volume: 152A
Issue / Number: 10
Start Page: 2651
End Page: 2655
Document Type: Article
ID: 533107.0
 
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Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis
Authors: Kariminejad, Ariana; Kariminejad, Roxana; Tzschach, Andreas; Ullmann, Reinhard; Ahmed, Alisho; Asghari-Roodsari, Alaleh; Salehpour, Shadab; Afroozan, Fariba; Ropers, Hans-Hilger; Kariminejad, Mohammad Hasan
Date of Publication (YYYY-MM-DD): 2009-07
Title of Journal: American Journal of Medical Genetics Part A
Volume: 149
Issue / Number: 7
Start Page: 1544
End Page: 1549
Document Type: Article
ID: 472586.0
Entries: 1-2  
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