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P Gallano

Showing results (1-10 of 46) with videos related to

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Prenatal Diagnosis|January 1, 1984
A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnosesA Boué, P Gallano
Medicina Clinica|April 14, 1990
[Molecular genetics in the research and diagnosis of human pathology]Z Estivill, V Nunes, P Gallano
Neurologia (Barcelona, Spain)|December 1, 1995
[Dystrophinopathies]P Gallano, A Lasa, M Baiget
Neurologia (Barcelona, Spain)|October 1, 1991
[Molecular genetics in neurology (II). Analysis of the human genome]F Palau, M Baiget, P Gallano
Prenatal Diagnosis|September 1, 1986
Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the European Collaborative Prenatal Diagnosis CentresA Daniel, A Boué, P Gallano
Neurologia (Barcelona, Spain)|August 1, 1991
[Molecular genetics in neurology (I). Diagnostic strategies in the genotypic study of monogenic hereditary pathology]M Baiget, P Gallano, F Palau
Human Mutation|January 1, 1997
Three novel point mutations in the dystrophin gene in DMD patientsA Lasa, P Gallano, M Baiget
Neurologia (Barcelona, Spain)|October 1, 1989
[Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers]M Baiget, E del Río, P Gallano
Neurologia (Barcelona, Spain)|November 1, 1991
[Molecular genetics in neurology (III). Contribution to the knowledge of molecular pathology]M P Gallano, M Baiget, F Palau
Clinical Genetics|September 1, 1995
A novel insertional mutation of a single base on exon 12 of the dystrophin geneA Lasa, P Gallano, J Colomer, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|January 1, 1984
A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnosesA Boué, P Gallano
Medicina Clinica|April 14, 1990
[Molecular genetics in the research and diagnosis of human pathology]Z Estivill, V Nunes, P Gallano
Neurologia (Barcelona, Spain)|December 1, 1995
[Dystrophinopathies]P Gallano, A Lasa, M Baiget
Neurologia (Barcelona, Spain)|October 1, 1991
[Molecular genetics in neurology (II). Analysis of the human genome]F Palau, M Baiget, P Gallano
Prenatal Diagnosis|September 1, 1986
Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the European Collaborative Prenatal Diagnosis CentresA Daniel, A Boué, P Gallano
Neurologia (Barcelona, Spain)|August 1, 1991
[Molecular genetics in neurology (I). Diagnostic strategies in the genotypic study of monogenic hereditary pathology]M Baiget, P Gallano, F Palau
Human Mutation|January 1, 1997
Three novel point mutations in the dystrophin gene in DMD patientsA Lasa, P Gallano, M Baiget
Neurologia (Barcelona, Spain)|October 1, 1989
[Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers]M Baiget, E del Río, P Gallano
Neurologia (Barcelona, Spain)|November 1, 1991
[Molecular genetics in neurology (III). Contribution to the knowledge of molecular pathology]M P Gallano, M Baiget, F Palau
Clinical Genetics|September 1, 1995
A novel insertional mutation of a single base on exon 12 of the dystrophin geneA Lasa, P Gallano, J Colomer, et al.
Pageof 5