M Jeanpierre|C Junien - JoVE Visualize

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Circulation|March 2, 1999

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophyA Lazarus, J Varin, Z Ounnoughene, et al.

Nature Genetics|November 1, 1994

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25G Collod, M C Babron, G Jondeau, et al.

Annals of Human Genetics|May 1, 1987

The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.

Cytogenetics and Cell Genetics|July 7, 1999

Abnormal methylation does not prevent X inactivation in ICF patientsD Bourc'his, P Miniou, M Jeanpierre, et al.

Genomics|May 15, 1994

Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic mapP Couillin, E Le Guern, A Vignal, et al.

Human Molecular Genetics|October 9, 2001

Defective satellite cells in congenital myotonic dystrophyD Furling, L Coiffier, V Mouly, et al.

Human Genetics|January 1, 1985

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.

Annales D'Endocrinologie|April 6, 1999

Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasiaJ C Fournet, V Verkarre, P De Lonlay, et al.

American Journal of Human Genetics|July 1, 1995

Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.

European Journal of Human Genetics : EJHG|October 22, 1998

Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan geneA Lasa, F Piccolo, C de Diego, et al.

Pageof 24

Showing results (171-180 of 232) with videos related to

Sort By:

Pageof 24

Circulation|March 2, 1999

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophyA Lazarus, J Varin, Z Ounnoughene, et al.

Nature Genetics|November 1, 1994

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25G Collod, M C Babron, G Jondeau, et al.

Annals of Human Genetics|May 1, 1987

The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.

Cytogenetics and Cell Genetics|July 7, 1999

Abnormal methylation does not prevent X inactivation in ICF patientsD Bourc'his, P Miniou, M Jeanpierre, et al.

Genomics|May 15, 1994

Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic mapP Couillin, E Le Guern, A Vignal, et al.

Human Molecular Genetics|October 9, 2001

Defective satellite cells in congenital myotonic dystrophyD Furling, L Coiffier, V Mouly, et al.

Human Genetics|January 1, 1985

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.

Annales D'Endocrinologie|April 6, 1999

Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasiaJ C Fournet, V Verkarre, P De Lonlay, et al.

American Journal of Human Genetics|July 1, 1995

Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.

European Journal of Human Genetics : EJHG|October 22, 1998

Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan geneA Lasa, F Piccolo, C de Diego, et al.

Pageof 24