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P Gallano

Showing results (11-20 of 46) with videos related to

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Anales Espanoles De Pediatria|April 1, 1992
[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome]E Tizzano Ferrari, P Gallano Petit, M Baiget Bastus
European Journal of Pediatrics|July 1, 1994
Severe mental retardation in a young boy with an in-frame deletion in the dystrophin geneJ Colomer, P Gallano, L V Nicholson, et al.
Human Genetics|January 1, 1985
The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specificM Jeanpierre, D Weil, P Gallano, et al.
Anales Espanoles De Pediatria|July 1, 1989
[Contribution of molecular genetics to the detection of carriers of severe genetic diseases]M Baiget Bastus, X Estivill Palleja, P Gallano Petit, et al.
Revista De Neurologia|June 1, 2002
[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]J Eirís-Puñal, E Pintos-Martínez, A Lasa, et al.
Journal of Medical Genetics|March 1, 1991
DMD carrier detection in a female with mosaic Turner's syndromeM Baiget, E Tizzano, V Volpini, et al.
American Journal of Human Genetics|May 1, 1989
Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRPX Estivill, C McLean, V Nunes, et al.
Revista De Neurologia|June 8, 2001
[Early onset adhalinopathy (LGMD2D) mimicking congenital muscular dystrophy]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Human Genetics|October 1, 1989
Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locusV Nunes, T Casals, P Gallano, et al.
Anales Espanoles De Pediatria|February 1, 1988
[Detection of carriers and diagnosis of Duchenne's muscular dystrophy by DNA analysis]V Nunes Martínez, P Gallano Petit, E del Río Conde, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Anales Espanoles De Pediatria|April 1, 1992
[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome]E Tizzano Ferrari, P Gallano Petit, M Baiget Bastus
European Journal of Pediatrics|July 1, 1994
Severe mental retardation in a young boy with an in-frame deletion in the dystrophin geneJ Colomer, P Gallano, L V Nicholson, et al.
Human Genetics|January 1, 1985
The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specificM Jeanpierre, D Weil, P Gallano, et al.
Anales Espanoles De Pediatria|July 1, 1989
[Contribution of molecular genetics to the detection of carriers of severe genetic diseases]M Baiget Bastus, X Estivill Palleja, P Gallano Petit, et al.
Revista De Neurologia|June 1, 2002
[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]J Eirís-Puñal, E Pintos-Martínez, A Lasa, et al.
Journal of Medical Genetics|March 1, 1991
DMD carrier detection in a female with mosaic Turner's syndromeM Baiget, E Tizzano, V Volpini, et al.
American Journal of Human Genetics|May 1, 1989
Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRPX Estivill, C McLean, V Nunes, et al.
Revista De Neurologia|June 8, 2001
[Early onset adhalinopathy (LGMD2D) mimicking congenital muscular dystrophy]M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
Human Genetics|October 1, 1989
Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locusV Nunes, T Casals, P Gallano, et al.
Anales Espanoles De Pediatria|February 1, 1988
[Detection of carriers and diagnosis of Duchenne's muscular dystrophy by DNA analysis]V Nunes Martínez, P Gallano Petit, E del Río Conde, et al.
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