Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU. (2017)

First Author: Depienne C

Attributed to: MRC Centre for Neurodevelopmental Disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00439-017-1772-0

PubMed Identifier: 28283832

Publication URI: http://europepmc.org/abstract/MED/28283832

Type: Journal Article/Review

Volume: 136

Parent Publication: Human genetics

Issue: 4

ISSN: 0340-6717