Partial Monosomy14q Involving FOXG1 and NOVA1 in an Infant With Microcephaly, Seizures and Severe Developmental Delay
Molecular Cytogenetics - United Kingdom
doi 10.1186/s13039-016-0269-1
Full Text
Open PDFAbstract
Available in full text
Date
August 2, 2016
Authors
Publisher
Springer Science and Business Media LLC