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Showing results (61-70 of 71) with videos related to

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European Journal of Haematology|July 1, 1987
Chronic T-cell leukaemias. A variant of T-prolymphocytic leukaemias: morphological, immunological and clinical characterization of 2 casesF Lauria, R Foà, D Raspadori, et al.
Nature Genetics|November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann diseaseK Janssens, R Gershoni-Baruch, N Guañabens, et al.
Journal of Medical Genetics|February 5, 2002
A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insAS Saviozzi, A Saluto, A M Taylor, et al.
Neurology|January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaA Brussino, C Gellera, A Saluto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2009
A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathyA Brussino, G Vaula, C Cagnoli, et al.
Journal of Medical Genetics|April 4, 2000
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13K Janssens, R Gershoni-Baruch, E Van Hul, et al.
European Journal of Neurology|April 8, 2009
Mutations in the lamin B1 gene are not present in multiple sclerosisA Brussino, S D'Alfonso, C Cagnoli, et al.
European Journal of Neurology|December 8, 2009
A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutationsA Brussino, G Vaula, C Cagnoli, et al.
Journal of Medical Genetics|May 17, 2005
Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatmentK Janssens, F Vanhoenacker, M Bonduelle, et al.
Genes, Chromosomes & Cancer|January 1, 1996
Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomasC Carbonara, L Longa, E Grosso, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
European Journal of Haematology|July 1, 1987
Chronic T-cell leukaemias. A variant of T-prolymphocytic leukaemias: morphological, immunological and clinical characterization of 2 casesF Lauria, R Foà, D Raspadori, et al.
Nature Genetics|November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann diseaseK Janssens, R Gershoni-Baruch, N Guañabens, et al.
Journal of Medical Genetics|February 5, 2002
A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insAS Saviozzi, A Saluto, A M Taylor, et al.
Neurology|January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaA Brussino, C Gellera, A Saluto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2009
A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathyA Brussino, G Vaula, C Cagnoli, et al.
Journal of Medical Genetics|April 4, 2000
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13K Janssens, R Gershoni-Baruch, E Van Hul, et al.
European Journal of Neurology|April 8, 2009
Mutations in the lamin B1 gene are not present in multiple sclerosisA Brussino, S D'Alfonso, C Cagnoli, et al.
European Journal of Neurology|December 8, 2009
A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutationsA Brussino, G Vaula, C Cagnoli, et al.
Journal of Medical Genetics|May 17, 2005
Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatmentK Janssens, F Vanhoenacker, M Bonduelle, et al.
Genes, Chromosomes & Cancer|January 1, 1996
Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomasC Carbonara, L Longa, E Grosso, et al.
Pageof 8