De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. (2018)
Attributed to:
Developing diagnostic methods for clinical genetics - phenotyping from faces in photos.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2018.04.014
PubMed Identifier: 29861108
Publication URI: http://europepmc.org/abstract/MED/29861108
Type: Journal Article/Review
Volume: 102
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297