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Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome. (2024)

First Author: Baena N

Attributed to: Identifying unique regulatory elements related to polymorphic imprinting and gestational aging in the placenta funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13148-024-01652-8

PubMed Identifier: 38715103

Publication URI: http://europepmc.org/abstract/MED/38715103

Type: Journal Article/Review

Volume: 16

Parent Publication: Clinical epigenetics

Issue: 1

ISSN: 1868-7075