reference/21951463

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21951463

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endingPage	27
issn	1096-8628 0148-7299
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pageRange	19-27
publicationName	American Journal of Medical Genetics
startingPage	19
bibliographicCitation	Munnes M, Fanaei S, Schmitz B, Muiznieks I, Holschneider AM, Doerfler W. Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes. Am J Med Genet. 2000 Sep 04;94(1):19–27. doi: 10.1002/1096-8628(20000904)94:1<19::aid-ajmg5>3.0.co;2-k. PMID: 10982477.
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date	2000-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/10982477 https://doi.org/10.1002/1096-8628%2820000904%2994:1%3C19::aid-ajmg5%3E3.0.co%3B2-k
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Familial form of Hirschsprung disease: Nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes
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