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A González-Meneses

Showing results (1-10 of 7) with videos related to

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Anales Espanoles De Pediatria|March 1, 1976
[Congenital syphilis (author's transl)]A González-Meneses, I G De Terreros
Anales Espanoles De Pediatria|December 1, 1976
[Tumor committee and pediatric oncology. Importance for management of infantile neoplasias (author's transl)]A González Meneses, A M Alvarez Silván
Revista De Neurologia|September 29, 2000
[Cerebral seizures in neonatal period: semiology, evolution and factors of influence]M Rufo-Campos, A González Meneses-López, C Rangel-Pineda
Anales Espanoles De Pediatria|November 1, 1975
[Smith-Lemli-Opitz syndrome. Cardiologic considerations (author's transl)]I Gómez de Terreros, C Cintado Bueno, S Ariza Almeida, 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.
Anales Espanoles De Pediatria|November 27, 1999
[Neonatal candidiasis and liposomal amphotericin B treatment: our experience]P Carrasco Sánchez, M L Castillo Montero, A Bejarano Palma, et al.
Journal of Medical Genetics|March 7, 2009
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotypeT Kleefstra, W A van Zelst-Stams, W M Nillesen, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Anales Espanoles De Pediatria|March 1, 1976
[Congenital syphilis (author's transl)]A González-Meneses, I G De Terreros
Anales Espanoles De Pediatria|December 1, 1976
[Tumor committee and pediatric oncology. Importance for management of infantile neoplasias (author's transl)]A González Meneses, A M Alvarez Silván
Revista De Neurologia|September 29, 2000
[Cerebral seizures in neonatal period: semiology, evolution and factors of influence]M Rufo-Campos, A González Meneses-López, C Rangel-Pineda
Anales Espanoles De Pediatria|November 1, 1975
[Smith-Lemli-Opitz syndrome. Cardiologic considerations (author's transl)]I Gómez de Terreros, C Cintado Bueno, S Ariza Almeida, 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.
Anales Espanoles De Pediatria|November 27, 1999
[Neonatal candidiasis and liposomal amphotericin B treatment: our experience]P Carrasco Sánchez, M L Castillo Montero, A Bejarano Palma, et al.
Journal of Medical Genetics|March 7, 2009
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotypeT Kleefstra, W A van Zelst-Stams, W M Nillesen, et al.
Pageof 1