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HARVARD Citation
Simonis, N. et al. (2013). FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. Journal of medical genetics. 50 (9), pp. 585-592. [Online].
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Simonis, N. et al. (2013). FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. Journal of medical genetics. 50 (9), pp. 585-592. [Online].