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L Mandel

Showing results (411-420 of 451) with videos related to

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American Journal of Human Genetics|October 1, 1996
Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in malesV Biancalana, L Taine, J C Bouix, et al.
Human Genetics|December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemiaS Guioli, B Arveiler, B Bardoni, et al.
Folia Microbiologica|January 1, 1995
The gut as a lymphoepithelial organ: the role of intestinal epithelial cells in mucosal immunityH Tlaskalová-Hogenová, M A Farré-Castany, R Stĕpánková, et al.
Nature|May 10, 1979
The ovalbumin gene region: common features in the organisation of three genes expressed in chicken oviduct under hormonal controlA Royal, A Garapin, B Cami, et al.
American Journal of Clinical Pathology|May 12, 1998
Teaching the clinical interpretation of peripheral blood smears to a second-year medical school class using the PeripheralBlood-Tutor computer programB Wood, L Mandel, D Schaad, et al.
The Journal of Sexual Medicine|September 20, 2024
The impact of Marfan syndrome and Ehlers-Danlos syndrome on the risk of penile fracture in patients between 18 and 45 yearsKaushik P Kolanukuduru, Asher L Mandel, Rishabh K Simhal, et al.
International Journal of Impotence Research|May 30, 2024
Marfan's syndrome is associated with a greater risk of Peyronie's disease: a case-control study of the TriNetX databaseKaushik P Kolanukuduru, Asher L Mandel, Rishabh K Simhal, et al.
American Journal of Human Genetics|March 1, 1985
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locusB de Martinville, L M Kunkel, G Bruns, et al.
American Journal of Medical Genetics|July 15, 1994
Sixth international workshop on the fragile X and X-linked mental retardationG R Sutherland, W T Brown, R Hagerman, et al.
Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.
Pageof 46

Showing results (411-420 of 451) with videos related to

Sort By:
Pageof 46
American Journal of Human Genetics|October 1, 1996
Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in malesV Biancalana, L Taine, J C Bouix, et al.
Human Genetics|December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemiaS Guioli, B Arveiler, B Bardoni, et al.
Folia Microbiologica|January 1, 1995
The gut as a lymphoepithelial organ: the role of intestinal epithelial cells in mucosal immunityH Tlaskalová-Hogenová, M A Farré-Castany, R Stĕpánková, et al.
Nature|May 10, 1979
The ovalbumin gene region: common features in the organisation of three genes expressed in chicken oviduct under hormonal controlA Royal, A Garapin, B Cami, et al.
American Journal of Clinical Pathology|May 12, 1998
Teaching the clinical interpretation of peripheral blood smears to a second-year medical school class using the PeripheralBlood-Tutor computer programB Wood, L Mandel, D Schaad, et al.
The Journal of Sexual Medicine|September 20, 2024
The impact of Marfan syndrome and Ehlers-Danlos syndrome on the risk of penile fracture in patients between 18 and 45 yearsKaushik P Kolanukuduru, Asher L Mandel, Rishabh K Simhal, et al.
International Journal of Impotence Research|May 30, 2024
Marfan's syndrome is associated with a greater risk of Peyronie's disease: a case-control study of the TriNetX databaseKaushik P Kolanukuduru, Asher L Mandel, Rishabh K Simhal, et al.
American Journal of Human Genetics|March 1, 1985
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locusB de Martinville, L M Kunkel, G Bruns, et al.
American Journal of Medical Genetics|July 15, 1994
Sixth international workshop on the fragile X and X-linked mental retardationG R Sutherland, W T Brown, R Hagerman, et al.
Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.
Pageof 46