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Showing results (221-230 of 388) with videos related to

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Journal of Medical Genetics|October 4, 2005
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilitiesJ B Ravnan, J H Tepperberg, P Papenhausen, et al.
Genomics|November 20, 1995
LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2O Reiner, I Bar-Am, T Sapir, et al.
Human Molecular Genetics|February 1, 1997
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3S S Chong, S D Pack, A V Roschke, et al.
Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.
Plos One|June 22, 2012
Human preferences for symmetry: subjective experience, cognitive conflict and cortical brain activityDavid W Evans, Patrick T Orr, Steven M Lazar, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1992
Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14M Labuda, T M Fujiwara, M V Ross, et al.
The Journal of the Acoustical Society of America|February 9, 2010
Polycrystalline gamma-plutonium's elastic moduli versus temperatureI Stroe, J B Betts, A Trugman, et al.
Human Molecular Genetics|May 16, 2009
Segmental duplications mediate novel, clinically relevant chromosome rearrangementsM Katharine Rudd, Julia Keene, Brian Bunke, et al.
Genomics|July 3, 2003
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23Hirobumi Sugawara, Naoki Harada, Tomoko Ida, et al.
American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.
Pageof 39

Showing results (221-230 of 388) with videos related to

Sort By:
Pageof 39
Journal of Medical Genetics|October 4, 2005
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilitiesJ B Ravnan, J H Tepperberg, P Papenhausen, et al.
Genomics|November 20, 1995
LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2O Reiner, I Bar-Am, T Sapir, et al.
Human Molecular Genetics|February 1, 1997
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3S S Chong, S D Pack, A V Roschke, et al.
Journal of Medical Genetics|January 3, 2001
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14P Ungaro, S L Christian, J A Fantes, et al.
Plos One|June 22, 2012
Human preferences for symmetry: subjective experience, cognitive conflict and cortical brain activityDavid W Evans, Patrick T Orr, Steven M Lazar, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1992
Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14M Labuda, T M Fujiwara, M V Ross, et al.
The Journal of the Acoustical Society of America|February 9, 2010
Polycrystalline gamma-plutonium's elastic moduli versus temperatureI Stroe, J B Betts, A Trugman, et al.
Human Molecular Genetics|May 16, 2009
Segmental duplications mediate novel, clinically relevant chromosome rearrangementsM Katharine Rudd, Julia Keene, Brian Bunke, et al.
Genomics|July 3, 2003
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23Hirobumi Sugawara, Naoki Harada, Tomoko Ida, et al.
American Journal of Human Genetics|July 1, 1995
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patientsS L Christian, W P Robinson, B Huang, et al.
Pageof 39