FGFR1mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly-Reference-Cited by-同舟云学术

FGFR1mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

Published:2013-06-28 Issue:9 Volume:50 Page:585-592
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Simonis Nicolas,Migeotte Isabelle,Lambert Nelle,Perazzolo Camille,de Silva Deepthi C,Dimitrov Boyan,Heinrichs Claudine,Janssens Sandra,Kerr Bronwyn,Mortier Geert,Van Vliet Guy,Lepage Philippe,Casimir Georges,Abramowicz Marc,Smits Guillaume,Vilain Catheline

Publisher

BMJ

Subject

Genetics(clinical),Genetics

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3. A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24;de Mollerat;Hum Mol Genet,2003

4. Hypertelorism associated with holoprosencephaly and ectrodactyly;Hartsfield;J Clin Dysmorphol,1984

5. Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review;Vilain;Am J Med Genet A,2009

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