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Q38806007-19BFC772-8F06-4F03-9400-A2E4993B5878
Q38806007-19BFC772-8F06-4F03-9400-A2E4993B5878
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Statement
http://www.wikidata.org/entity/statement/Q38806007-19BFC772-8F06-4F03-9400-A2E4993B5878
Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1.
P2860
Q38806007-19BFC772-8F06-4F03-9400-A2E4993B5878
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38806007-19BFC772-8F06-4F03-9400-A2E4993B5878
rank
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type
BestRank
Statement
wasDerivedFrom
56193d23f55587ccc93009b553c45704e9307756
P2860
Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation