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Publikováno v:
Acta Pediátrica de México, Vol 34, Iss 1, Pp 43-47 (2014)
Pfeiffer syndrome is a rare autosomal dominant disease that affects almost 1 out of every 100,000 live newborns, and it is associated with craniosynostosis, broad and deviated thumbs and big toes, and partial syndactyly in hands and feet. Three types
Externí odkaz:
https://doaj.org/article/71f3434754e14613a82b6a958d3bc55b
Autor:
Roldán-Arce, Jorge1, Villarroel-Cortés, Camilo2 camiloevc@yahoo.com
Publikováno v:
Acta Pediatrica de Mexico. ene/feb2013, Vol. 34 Issue 1, p43-47. 5p.