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Q21245642-3D036CAC-4E36-4F9B-94AF-C1D24B744772
Q21245642-3D036CAC-4E36-4F9B-94AF-C1D24B744772
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http://www.wikidata.org/entity/statement/Q21245642-3D036CAC-4E36-4F9B-94AF-C1D24B744772
Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).
P2860
Q21245642-3D036CAC-4E36-4F9B-94AF-C1D24B744772
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21245642-3D036CAC-4E36-4F9B-94AF-C1D24B744772
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wasDerivedFrom
39b4f441c7518f16be16b4a9dd433422ac73eb25
P2860
Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families