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Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposis. (2019)

First Author: Gregory LC

Attributed to: Human Developmental Biology Resource (HDBR): an embryonic and fetal tissue bank for functional genetics and cell-based research funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1210/jc.2019-00631

PubMed Identifier: 31504653

Publication URI: http://europepmc.org/abstract/MED/31504653

Type: Journal Article/Review

Volume: 104

Parent Publication: The Journal of clinical endocrinology and metabolism

Issue: 12

ISSN: 0021-972X