reference/34187691

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/34187691

Outgoing Links

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contentType	Case Reports\|Review
endingPage	538
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pageRange	535-538
publicationName	Taiwanese Journal of Obstetrics and Gynecology
startingPage	535
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bibliographicCitation	Qiu Z, Chang W, Chou Y, Wen K, Ziying Y, Yuen K, Cai X, Chang T, Lai H, Sung P. Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature. Taiwanese Journal of Obstetrics and Gynecology. 2022 May;61(3):535–8. doi: 10.1016/j.tjog.2022.03.025.
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date	202205
identifier	https://pubmed.ncbi.nlm.nih.gov/35595454 https://doi.org/10.1016/j.tjog.2022.03.025
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature
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