JBCGenetics
 2018
DOI: 10.24911/jbcgenetics/183-1532358706
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A new case of de novo chromosome 19p13.12 deletion in an Omani girl with multiple congenital anomalies: a first case report from Oman

Musallam Al‐Araimi1,
Aliya Al-Hosni2,
Ali Ahmed Al-Yahmadi3
et al.
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