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- W1930346508 abstract "HOX genes play a fundamental role in the development of the vertebrate central nervous system, axial skeleton, limbs, gut, urogenital tract and external genitalia, but it is only in the last 4 years that mutations in two of the 39 human HOX genes have been shown to cause congenital malformations; HOXD13, which is mutated in synpolydactyly, and HOXA13, which is mutated in Hand-Foot-Genital syndrome. Here we review the mutations already identified in these two genes, consider how these mutations may act, and discuss the possibility that further mutations remain to be discovered both in developmental disorders and in cancer." @default.
- W1930346508 created "2016-06-24" @default.
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- W1930346508 date "2001-01-01" @default.
- W1930346508 modified "2023-10-18" @default.
- W1930346508 title "Human<i>HOX</i>gene mutations" @default.
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- W1930346508 doi "https://doi.org/10.1034/j.1399-0004.2001.590101.x" @default.
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