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Q40478474-52F328E2-BBAC-411F-988A-CFFDE7B4A841
Q40478474-52F328E2-BBAC-411F-988A-CFFDE7B4A841
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http://www.wikidata.org/entity/statement/Q40478474-52F328E2-BBAC-411F-988A-CFFDE7B4A841
A Novel Heterozygous Intragenic Sequence Variant in DLX6 Probably Underlies First Case of Autosomal Dominant Split-Hand/Foot Malformation Type 1.
P2860
Q40478474-52F328E2-BBAC-411F-988A-CFFDE7B4A841
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40478474-52F328E2-BBAC-411F-988A-CFFDE7B4A841
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wasDerivedFrom
fea66d3505e72a0229893e4885798af2ac7667cd
P2860
A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence