Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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1. Mid1/Mid2 expression in craniofacial development and a literature review of X‐linked Opitz syndrome;Molecular Genetics & Genomic Medicine;2015-12-12
2. Rbm24a and Rbm24b Are Required for Normal Somitogenesis;PLoS ONE;2014-08-29
3. Wolf-Hirschhorn Syndrome (WHS) – Literature Review on the Features of the Syndrome;Advances in Clinical and Experimental Medicine;2014
4. Operative Korrektur der symptomatischen A. lusoria in zwei Fällen bei Verwandten ersten Grades;Gefässchirurgie;2010-04-10
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