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G Rodríguez Criado

Showing results (1-10 of 10) with videos related to

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Anales De Pediatria (Barcelona, Spain : 2003)|November 23, 2011
[New X linked mental retardation syndrome]G Rodríguez Criado
Revista De Neurologia|April 25, 2000
[Corpus callosum agenesis and epileptic seizures]M Nieto-Barrera, G Rodríguez-Criado, M Carballo
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Familial deletion of 22q11.2G Rodríguez Criado, J Gruesomontero, A Delicado Navarro
Clinical Dysmorphology|October 26, 1999
A second family with Micro syndromeG Rodríguez Criado, M Rufo, I Gómez de Terreros
American Journal of Medical Genetics. Part A|January 11, 2003
Clinical variability of type II sialidosis by C808T mutationG Rodríguez Criado, A V Pshezhetsky, A Rodríguez Becerra, et al.
Anales Espanoles De Pediatria|April 1, 1988
[Desquamative interstitial pneumonia in an infant]A Pavón Delgado, G Rodríguez Criado, F Borderas Naranjo, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
First report of a patient with a mixoploidy 47,XXX/94,XXXXXXG Rodríguez Criado, E Galán Gómez, E F Tizzano, et al.
Anales Espanoles De Pediatria|November 1, 1977
[Treatment of infantile hydrocephalus with isosorbide dinitrate (author's transl)]M Nieto Barrera, R Candáu Fernández-Mensaque, M Rufo Campos, et al.
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
X-linked hydrocephalus: another two families with an L1 mutationG Rodríguez Criado, A Pérez Aytés, F Martínez, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Anales De Pediatria (Barcelona, Spain : 2003)|November 23, 2011
[New X linked mental retardation syndrome]G Rodríguez Criado
Revista De Neurologia|April 25, 2000
[Corpus callosum agenesis and epileptic seizures]M Nieto-Barrera, G Rodríguez-Criado, M Carballo
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Familial deletion of 22q11.2G Rodríguez Criado, J Gruesomontero, A Delicado Navarro
Clinical Dysmorphology|October 26, 1999
A second family with Micro syndromeG Rodríguez Criado, M Rufo, I Gómez de Terreros
American Journal of Medical Genetics. Part A|January 11, 2003
Clinical variability of type II sialidosis by C808T mutationG Rodríguez Criado, A V Pshezhetsky, A Rodríguez Becerra, et al.
Anales Espanoles De Pediatria|April 1, 1988
[Desquamative interstitial pneumonia in an infant]A Pavón Delgado, G Rodríguez Criado, F Borderas Naranjo, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
First report of a patient with a mixoploidy 47,XXX/94,XXXXXXG Rodríguez Criado, E Galán Gómez, E F Tizzano, et al.
Anales Espanoles De Pediatria|November 1, 1977
[Treatment of infantile hydrocephalus with isosorbide dinitrate (author's transl)]M Nieto Barrera, R Candáu Fernández-Mensaque, M Rufo Campos, et al.
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
X-linked hydrocephalus: another two families with an L1 mutationG Rodríguez Criado, A Pérez Aytés, F Martínez, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 1