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2013 | 1 |
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FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
J Med Genet. 2013 Sep;50(9):585-92. doi: 10.1136/jmedgenet-2013-101603. Epub 2013 Jun 28.
J Med Genet. 2013.
PMID: 23812909
Free PMC article.
Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review.
Vilain C, Mortier G, Van Vliet G, Dubourg C, Heinrichs C, de Silva D, Verloes A, Baumann C.
Vilain C, et al.
Am J Med Genet A. 2009 Jul;149A(7):1476-81. doi: 10.1002/ajmg.a.32678.
Am J Med Genet A. 2009.
PMID: 19504604
Free article.
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