reference/35930352

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/35930352

Outgoing Links

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contentType	Journal Article
issn	1098-3600
issueIdentifier	7
pageRange	100839-
publicationName	Genetics in medicine : official journal of the American College of Medical Genetics
startingPage	100839
bibliographicCitation	Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, Faoucher M, Kaplan J, Procopio R, Saunders CJ, Cohen ASA, Lemire G, Sacharow S, O'Donnell-Luria A, Segal RJ, Kianmahd Shamshoni J, Schweitzer D, Ebrahimi-Fakhari D, Monaghan K, Palculict TB, Napier MP, Tao A, Isidor B, Moradkhani K, Reis A, Sticht H; Care4Rare Canada, Chung WK, Zweier C. LHX2 haploinsufficiency causes a variable neurodevelopmental disorder. Genet Med. 2023 Jul;25(7):100839. doi: 10.1016/j.gim.2023.100839. PMID: 37057675.
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date	202307
identifier	https://pubmed.ncbi.nlm.nih.gov/37057675 https://doi.org/10.1016/j.gim.2023.100839
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	LHX2 haploinsufficiency causes a variable neurodevelopmental disorder
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