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P Gallano

Showing results (21-30 of 46) with videos related to

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Human Genetics|May 1, 1986
The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1)C Huerre-Jeanpierre, I Henry, M Bernard, et al.
British Journal of Haematology|May 1, 1992
High prevalence of the beta-thalassaemia nonsense 37 mutation in Catalonians from the Ebro deltaP Gallano, E Girodon, N Ghanem, et al.
Annals of Human Genetics|July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32I Henry, P Gallano, C Besmond, et al.
European Journal of Medical Genetics|July 28, 2011
LMNA mutation in progeroid syndrome in association with strokesL Gonzalez-Quereda, V Delgadillo, J Juan-Mateu, et al.
Annales De Genetique|January 1, 1987
[Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data]C Junien, J Boué, C Duros, et al.
European Journal of Neurology|June 11, 2011
Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated alleleM Meznaric, L Gonzalez-Quereda, E Gallardo, et al.
Journal of Neurology|October 20, 1999
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesC de Diego, J Gámez, E Plassart-Schiess, et al.
Human Genetics|September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populationsX Estivill, P Gasparini, G Novelli, et al.
Neurology|February 9, 2007
Symptomatic dysferlin gene mutation carriers: characterization of two casesI Illa, N De Luna, R Domínguez-Perles, et al.
Neuromuscular Disorders : NMD|December 17, 2008
A new phenotype of dysferlinopathy with congenital onsetC Paradas, L González-Quereda, N De Luna, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Human Genetics|May 1, 1986
The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1)C Huerre-Jeanpierre, I Henry, M Bernard, et al.
British Journal of Haematology|May 1, 1992
High prevalence of the beta-thalassaemia nonsense 37 mutation in Catalonians from the Ebro deltaP Gallano, E Girodon, N Ghanem, et al.
Annals of Human Genetics|July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32I Henry, P Gallano, C Besmond, et al.
European Journal of Medical Genetics|July 28, 2011
LMNA mutation in progeroid syndrome in association with strokesL Gonzalez-Quereda, V Delgadillo, J Juan-Mateu, et al.
Annales De Genetique|January 1, 1987
[Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data]C Junien, J Boué, C Duros, et al.
European Journal of Neurology|June 11, 2011
Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated alleleM Meznaric, L Gonzalez-Quereda, E Gallardo, et al.
Journal of Neurology|October 20, 1999
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesC de Diego, J Gámez, E Plassart-Schiess, et al.
Human Genetics|September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populationsX Estivill, P Gasparini, G Novelli, et al.
Neurology|February 9, 2007
Symptomatic dysferlin gene mutation carriers: characterization of two casesI Illa, N De Luna, R Domínguez-Perles, et al.
Neuromuscular Disorders : NMD|December 17, 2008
A new phenotype of dysferlinopathy with congenital onsetC Paradas, L González-Quereda, N De Luna, et al.
Pageof 5