Open AccessA Rare Fındıng of Chromosome 22q11.2 Deletıon Syndrome: Multıcystıc Dysplastık Kıdney
Author(s) -
Fuat Buğrul,
Fahrettin Duymus
Publication year - 2019
Publication title -
çocuk dergisi / journal of child
Language(s) - English
Resource type - Journals
eISSN - 1302-9940
pISSN - 1308-8491
DOI - 10.5222/j.child.2019.76768
Subject(s) - digeorge syndrome , microdeletion syndrome , hypoplasia , medicine , hypoparathyroidism , chromosome , deletion syndrome , cyst , pathology , pediatrics , genetics , biology , gene , phenotype
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