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Q33403857-4126B70E-AECC-4DA7-AA6A-69F78844492D
Q33403857-4126B70E-AECC-4DA7-AA6A-69F78844492D
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http://www.wikidata.org/entity/statement/Q33403857-4126B70E-AECC-4DA7-AA6A-69F78844492D
Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis.
P2860
Q33403857-4126B70E-AECC-4DA7-AA6A-69F78844492D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33403857-4126B70E-AECC-4DA7-AA6A-69F78844492D
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wasDerivedFrom
566ce125d1d9d70bbb06c3a3463313218e8321f7
P2860
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development