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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

Volume: 93

Parent Publication: Clinical genetics

Issue: 4

ISSN: 0009-9163