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Q28066570-87138345-7558-4437-83EE-6B91FC1648E4
Q28066570-87138345-7558-4437-83EE-6B91FC1648E4
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http://www.wikidata.org/entity/statement/Q28066570-87138345-7558-4437-83EE-6B91FC1648E4
Genetic insights into the mechanisms of Fgf signaling
P2860
Q28066570-87138345-7558-4437-83EE-6B91FC1648E4
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http://www.wikidata.org/entity/statement/Q28066570-87138345-7558-4437-83EE-6B91FC1648E4
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c7f8587bec2167f586358c08fd0bf837bbc38ee2
P2860
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.