C Ramos Corrales - JoVE Visualize

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Anales Espanoles De Pediatria|January 1, 1993

[Study of the gene of Duchenne muscular dystrophy using PCR analysis]M Villamar López, E Fernández García, C Ramos Corrales, et al.

Anales Espanoles De Pediatria|April 1, 1987

[Prune belly syndrome with associated anomalies and chromosome changes (20 p+)]C Picardo López, C Ramos Corrales, J Bello González, et al.

Anales Espanoles De Pediatria|April 1, 1992

[Cytogenetic study of a family with 15p+ chromosomal plymorphism]A I Manzanal Martínez, M Robledo Batanero, C Ramos Corrales, et al.

Anales Espanoles De Pediatria|July 15, 1998

[Quick diagnosis of Prader-Willi and Angelman syndromes by means of methylation test by PCR]C Huerta Rivas, A Barabash Bustelo, J Gallego Merlo, et al.

Journal of Assisted Reproduction and Genetics|October 1, 2009

Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 geneM J Trujillo-Tiebas, M Fenollar-Cortés, I Lorda-Sánchez, et al.

Anales Espanoles De Pediatria|April 1, 1989

[Use of the recombinant DNA technic in studying cystic fibrosis in 14 Spanish families: detection of carriers and healthy subjects]E Fernández García, J Benítez Ortiz, M Villamar López, et al.

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Showing results (1-10 of 6) with videos related to

Sort By:

Pageof 1

Anales Espanoles De Pediatria|January 1, 1993

[Study of the gene of Duchenne muscular dystrophy using PCR analysis]M Villamar López, E Fernández García, C Ramos Corrales, et al.

Anales Espanoles De Pediatria|April 1, 1987

[Prune belly syndrome with associated anomalies and chromosome changes (20 p+)]C Picardo López, C Ramos Corrales, J Bello González, et al.

Anales Espanoles De Pediatria|April 1, 1992

[Cytogenetic study of a family with 15p+ chromosomal plymorphism]A I Manzanal Martínez, M Robledo Batanero, C Ramos Corrales, et al.

Anales Espanoles De Pediatria|July 15, 1998

[Quick diagnosis of Prader-Willi and Angelman syndromes by means of methylation test by PCR]C Huerta Rivas, A Barabash Bustelo, J Gallego Merlo, et al.

Journal of Assisted Reproduction and Genetics|October 1, 2009

Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 geneM J Trujillo-Tiebas, M Fenollar-Cortés, I Lorda-Sánchez, et al.

Anales Espanoles De Pediatria|April 1, 1989

[Use of the recombinant DNA technic in studying cystic fibrosis in 14 Spanish families: detection of carriers and healthy subjects]E Fernández García, J Benítez Ortiz, M Villamar López, et al.

Pageof 1