학술논문
Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus.
Document Type
Article
Author
Source
Journal of Medical Genetics; Jun2012, Vol. 49 Issue 6, p366-372, 7p, 1 Color Photograph, 1 Diagram, 2 Charts
Subject
Language
ISSN
00222593
Abstract
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