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Q44593621-C0D4C5F2-9037-4427-BB9C-898B3C8BDB0E
Q44593621-C0D4C5F2-9037-4427-BB9C-898B3C8BDB0E
BestRank
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http://www.wikidata.org/entity/statement/Q44593621-C0D4C5F2-9037-4427-BB9C-898B3C8BDB0E
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
P2860
Q44593621-C0D4C5F2-9037-4427-BB9C-898B3C8BDB0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44593621-C0D4C5F2-9037-4427-BB9C-898B3C8BDB0E
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wasDerivedFrom
b4d6ae9c75833cfc07736f1496a8e810ba47fb6b
P2860
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in Humans