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Microdeletion of 1p32-p31 involving NFIA in a patient with hypoplastic corpus callosum, ventriculomegaly, seizures and urinary tract defects

EUROPEAN JOURNAL OF MEDICAL GENETICS (2014)

Journal

EUROPEAN JOURNAL OF MEDICAL GENETICS

Volume 57, Issue 6, Pages 267-268

Publisher

ELSEVIER SCIENCE BV

DOI: 10.1016/j.ejmg.2014.03.004

Keywords

NFIA gene; Microdeletion; Chromosome 1p32-p31; Hypoplastic corpus callosum; CNS defect; Urinary tract defect

Categories

Genetics & Heredity

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