A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly (2018)

First Author: Ishida M

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/cge.13189

PubMed Identifier: 29205322

Publication URI: http://europepmc.org/abstract/MED/29205322

Type: Journal Article/Review

Parent Publication: Clinical Genetics

Issue: 4

ISSN: 0009-9163