reference/33843536

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/33843536

Outgoing Links

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contentType	Journal Article\|Research Support, N.I.H., Extramural
endingPage	696
issn	0022-2593 1468-6244
issueIdentifier	7
pageRange	691-696
publicationName	Journal of Medical Genetics
startingPage	691
bibliographicCitation	Bolkier Y, Barel O, Marek-Yagel D, Atias-Varon D, Kagan M, Vardi A, Mishali D, Katz U, Salem Y, Tirosh-Wagner T, Jacobson JM, Raas-Rothschild A, Chorin O, Eliyahu A, Sarouf Y, Shlomovitz O, Veber A, Shalva N, Javasky E, Ben Moshe Y, Staretz-Chacham O, Rechavi G, Mane S, Anikster Y, Vivante A, Pode-Shakked B. Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects. J Med Genet. 2022 Jul;59(7):691–6. doi: 10.1136/jmedgenet-2021-107775. PMID: 34215651.
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date	2021-07-02^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/34215651 https://doi.org/10.1136/jmedgenet-2021-107775
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4945 https://portal.issn.org/resource/ISSN/1468-6244 https://portal.issn.org/resource/ISSN/0022-2593
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
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