Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22.3p22.2. (2020)

First Author: Vendramini-Pittoli S
Attributed to:  Developmental Disorders: From Diagnosis to Mechanism via Cis-Regulation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1055/s-0039-3402047

PubMed Identifier: 32765930

Publication URI: http://europepmc.org/abstract/MED/32765930

Type: Journal Article/Review

Volume: 9

Parent Publication: Journal of pediatric genetics

Issue: 4

ISSN: 2146-460X