FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

BACKGROUND: Harstfield syndrome is the rare and unique association of holoprosencephaly (HPE) and ectrodactyly, with or without cleft lip and palate, and variable additional features. All the reported cases occurred sporadically. Although several causal genes of HPE and ectrodactyly have been identi...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Developmental Defects
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756455/
https://www.ncbi.nlm.nih.gov/pubmed/23812909
http://dx.doi.org/10.1136/jmedgenet-2013-101603

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756455/
https://www.ncbi.nlm.nih.gov/pubmed/23812909
http://dx.doi.org/10.1136/jmedgenet-2013-101603

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