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Added reference to claim: main subject (P921): multiple endocrine neoplasia type 2A (Q604075), #quickstatements; #temporary_batch_1576516256866
Set a claim value: title (P1476): The Hirschsprung's-multiple endocrine neoplasia connection
 
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label / enlabel / en
The Hirschsprung's-multiple endocrine neoplasia connection.
The Hirschsprung's-multiple endocrine neoplasia connection
label / astlabel / ast
 
The Hirschsprung's-multiple endocrine neoplasia connection
label / nllabel / nl
 
The Hirschsprung's-multiple endocrine neoplasia connection
description / astdescription / ast
artículu científicu
artículu científicu espublizáu en 2012
Property / titleProperty / title
The Hirschsprung's-multiple endocrine neoplasia connection. (English)
The Hirschsprung's-multiple endocrine neoplasia connection (English)
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Property / cites work: Mutational analysis of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung's disease / rank
 
Normal rank
Property / cites work: Mutational analysis of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung's disease / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: Total thyroidectomy for hereditary medullary thyroid carcinoma 12 years after correction of Hirschsprung's disease / rank
 
Normal rank
Property / cites work: Total thyroidectomy for hereditary medullary thyroid carcinoma 12 years after correction of Hirschsprung's disease / reference
 
stated in: PubMed
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Property / cites work: Gastrointestinal manifestations of Sipple syndrome in children / rank
 
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stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease / rank
 
Normal rank
Property / cites work: Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: Clinical presentations and RET protooncogene mutations in seven multiple endocrine neoplasia type 2 kindreds / rank
 
Normal rank
Property / cites work: Clinical presentations and RET protooncogene mutations in seven multiple endocrine neoplasia type 2 kindreds / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: RET alternate splicing influences the interaction of activated RET with the SH2 and PTB domains of Shc, and the SH2 domain of Grb2 / rank
 
Normal rank
Property / cites work: RET alternate splicing influences the interaction of activated RET with the SH2 and PTB domains of Shc, and the SH2 domain of Grb2 / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation / rank
 
Normal rank
Property / cites work: Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: Occurrence of MEN 2a in familial Hirschsprung's disease: a new indication for genetic testing of the RET proto-oncogene / rank
 
Normal rank
Property / cites work: Occurrence of MEN 2a in familial Hirschsprung's disease: a new indication for genetic testing of the RET proto-oncogene / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: Aganglionic megacolon, pheochromocytoma, megaloureter, and neurofibroma; co-occurrence of several neural abnormalities / rank
 
Normal rank
Property / cites work: Aganglionic megacolon, pheochromocytoma, megaloureter, and neurofibroma; co-occurrence of several neural abnormalities / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Property / cites work: A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease / rank
 
Normal rank
Property / cites work: A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/22584708
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Precision1 day
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