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Q24517956-7CC48954-E974-4F0B-BEE8-559B138B356D
Q24517956-7CC48954-E974-4F0B-BEE8-559B138B356D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24517956-7CC48954-E974-4F0B-BEE8-559B138B356D
Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23
P2860
Q24517956-7CC48954-E974-4F0B-BEE8-559B138B356D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24517956-7CC48954-E974-4F0B-BEE8-559B138B356D
rank
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type
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wasDerivedFrom
1617b9636766367b06d67de8bb0e018cf7e21c23
P2860
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient