Open AccessCase Report: Interstitial Deletion 21q22.13-Q22.3 in a Male Patient with Developmental Delay, Holoprosencephaly, Dysmorphic Features, and Multiple Congenital Anomalies
Author(s) -
Ibtessam R. Hussein
Publication year - 2015
Publication title -
journal of molecular biomarkers and diagnosis
Language(s) - English
Resource type - Journals
ISSN - 2155-9929
DOI - 10.4172/2155-9929.1000222
Subject(s) - holoprosencephaly , medicine , global developmental delay , pediatrics , genetics , bioinformatics , biology , gene , phenotype , fetus , pregnancy
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