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Revista De Neurologia|March 1, 2006
[Monogenic causes of X-linked mental retardation]E Guillén-Navarro, G Glóver-López
Revista De Neurologia|March 1, 2006
[Fragile X syndrome]G Glóver-López, E Guillén-Navarro
Clinical Dysmorphology|November 21, 1998
Acro-renal-ocular syndrome: expansion of the phenotypeE Guillén-Navarro, R Wallerstein, E Reich, et al.
Clinical Neurology and Neurosurgery|June 24, 1998
A new form of complicated hereditary spastic paraplegia with cataracts, atretic ear canals and hypopigmentationE Guillén-Navarro, R Wallerstein, E Moran, et al.
Annals of Human Genetics|October 8, 2004
Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyriaE Guillén-Navarro, P Carbonell, G Glover, et al.
European Journal of Medical Genetics|July 11, 2006
Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal originI López-Exposito, E Guillén-Navarro, J A Bafallíu, et al.
Archives of Dermatological Research|December 25, 2009
A compound heterozygous mutation in the EDAR gene in a Spanish family with autosomal recessive hypohidrotic ectodermal dysplasiaM R Moya-Quiles, M J Ballesta-Martínez, V López-González, et al.
Archives of Surgery (Chicago, Ill. : 1960)|September 16, 1999
Biliary duct injury: partial segment IV resection for intrahepatic reconstruction of biliary lesionsM A Mercado, H Orozco, L de la Garza, et al.
Journal of Gastrointestinal Surgery : Official Journal of the Society for Surgery of the Alimentary Tract|November 15, 2000
Small-diameter mesocaval shunts: a 10-year evaluationM A Mercado, H Orozco, E Guillén-Navarro, et al.
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