A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|8|1865-1871

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.8, 2015-08, pp. : 1865-1871

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