reference/1776792

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1776792

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	504
issn	1468-6244 0022-2593
issueIdentifier	7
pageRange	497-504
publicationName	Journal of Medical Genetics
startingPage	497
bibliographicCitation	Jeanpierre C, Macé G, Parisot M, Morinière V, Pawtowsky A, Benabou M, Martinovic J, Amiel J, Attié-Bitach T, Delezoide AL, Loget P, Blanchet P, Gaillard D, Gonzales M, Carpentier W, Nitschke P, Tores F, Heidet L, Antignac C, Salomon R; Société Française de Foetopathologie. RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. J Med Genet. 2011 Jul;48(7):497–504. doi: 10.1136/jmg.2010.088526. PMID: 21490379.
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date	2011-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/21490379 https://doi.org/10.1136/jmg.2010.088526
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects
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