FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly | Journal of Medical Genetics

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FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

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Cite this article as:: Simonis N, Migeotte I, Lambert N, et al

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

Journal of Medical Genetics 2013;50:585-592.