Author:
Mundlos Stefan,Horn Denise
Publisher
Springer Berlin Heidelberg
Reference4 articles.
1. Hartsfield JK Jr., Bixler D, DeMyer WE (1984) Hypertelorism associated with holoprosencephaly and ectrodactyly. J Clin Dysmorph 2:27–31
2. Konig R, Beeg T, Tariverdian G, Scheffer H, Bitter K (2003) Holoprosencephaly, bilateral cleft lip and palate and ectrodactyly: another case and follow up. Clin Dysmorph 12:221–225
3. Simonis N, Migeotte I, Lambert N, Perazzolo C, de Silva DC, Dimitrov B et al (2013) FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. J Med Genet 50:585–592
4. Vilain C, Mortier G, Van Vliet G, Dubourg C, Heinrichs C, de Silva D et al (2009) Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review. Am J Med Genet 149A:1476–1481