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Browsing by Author Heinrichs, C.
Showing results 1 to 2 of 2
Issue Date | Title | Author(s) |
2013 | FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly | Simonis, N.; Migeotte, I.; Lambert, N.; Perazzolo, C.; de Silva, D.C.; Dimitrov, B.; Heinrichs, C.; Janssens, S.; Kerr, B.; Mortier, G.; Van Vliet, G.; Lepage, P.; Casimir, G.; Abramowicz, M.; Smits, G.; Vilain, C. |
2009 | Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review | Vilain, C.; Mortier, G.; Van, G. V.; Dubourg, C.; Heinrichs, C.; de Silva, D.; Verloes, C. B. |