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C Junien

Showing results (241-250 of 284) with videos related to

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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.
Clinical Genetics|February 27, 2004
Identification of the first Lebanese mutation in the LPL gene and description of a rapid detection methodM Abifadel, S Jambart, D Allard, 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.
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1982
[Combination of external irradiation and interstitial curietherapy in epitheliomas of the mobile portion of the tongue and the floor of the mouth]M Bolla, J C Horiot, C Junien-Lavillauroy, 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.
Circulation|September 1, 1996
Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenonD Annane, P Merlet, H Radvanyi, et al.
Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2G Collod, M L Chu, T Sasaki, et al.
Pageof 29

Showing results (241-250 of 284) with videos related to

Sort By:
Pageof 29
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.
Clinical Genetics|February 27, 2004
Identification of the first Lebanese mutation in the LPL gene and description of a rapid detection methodM Abifadel, S Jambart, D Allard, 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.
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1982
[Combination of external irradiation and interstitial curietherapy in epitheliomas of the mobile portion of the tongue and the floor of the mouth]M Bolla, J C Horiot, C Junien-Lavillauroy, 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.
Circulation|September 1, 1996
Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenonD Annane, P Merlet, H Radvanyi, et al.
Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2G Collod, M L Chu, T Sasaki, et al.
Pageof 29