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Showing results (101-110 of 200) with videos related to

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Optics Express|November 3, 2017
Analysis of Ge micro-cavities with in-plane tensile strains above 2R W Millar, K Gallacher, J Frigerio, et al.
Genomics|February 28, 1998
Human FIGF: cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genesM Rocchigiani, M Lestingi, A Luddi, et al.
American Journal of Medical Genetics|September 6, 1996
Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locusK Muroya, T Ogata, N Matsuo, et al.
Human Molecular Genetics|October 1, 1994
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryoB Lutz, S Kuratani, E I Rugarli, et al.
Genomics|October 1, 1991
A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesisB Bardoni, O Zuffardi, S Guioli, et al.
American Journal of Medical Genetics|February 2, 1996
Autosomal dominant transmission of familial laterality defectsB Casey, B F Cuneo, C Vitali, et al.
Nature Genetics|November 4, 2000
The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsyM De Fusco, A Becchetti, A Patrignani, et al.
Human Molecular Genetics|July 1, 1994
A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22M C Wapenaar, M V Schiaffino, M T Bassi, et al.
Mechanisms of Development|September 3, 1999
Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain developmentA Bulfone, S Martinez, V Marigo, et al.
Nature Genetics|August 1, 1995
Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J miceE I Rugarli, D A Adler, G Borsani, et al.
Pageof 20

Showing results (101-110 of 200) with videos related to

Sort By:
Pageof 20
Optics Express|November 3, 2017
Analysis of Ge micro-cavities with in-plane tensile strains above 2R W Millar, K Gallacher, J Frigerio, et al.
Genomics|February 28, 1998
Human FIGF: cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genesM Rocchigiani, M Lestingi, A Luddi, et al.
American Journal of Medical Genetics|September 6, 1996
Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locusK Muroya, T Ogata, N Matsuo, et al.
Human Molecular Genetics|October 1, 1994
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryoB Lutz, S Kuratani, E I Rugarli, et al.
Genomics|October 1, 1991
A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesisB Bardoni, O Zuffardi, S Guioli, et al.
American Journal of Medical Genetics|February 2, 1996
Autosomal dominant transmission of familial laterality defectsB Casey, B F Cuneo, C Vitali, et al.
Nature Genetics|November 4, 2000
The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsyM De Fusco, A Becchetti, A Patrignani, et al.
Human Molecular Genetics|July 1, 1994
A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22M C Wapenaar, M V Schiaffino, M T Bassi, et al.
Mechanisms of Development|September 3, 1999
Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain developmentA Bulfone, S Martinez, V Marigo, et al.
Nature Genetics|August 1, 1995
Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J miceE I Rugarli, D A Adler, G Borsani, et al.
Pageof 20