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Human mutation

Showing results (831-840 of 6,545) with videos related to

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Human Mutation|December 7, 2007
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based arrayTeresita Díaz de Ståhl, Johanna Sandgren, Arkadiusz Piotrowski, et al.
Human Mutation|December 7, 2007
Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related diseaseAlessandro Pecci, Emanuele Panza, Núria Pujol-Moix, et al.
Human Mutation|February 14, 2006
Study of four genes belonging to the folate pathway: transcobalamin 2 is involved in the onset of non-syndromic cleft lip with or without cleft palateMarcella Martinelli, Luca Scapoli, Annalisa Palmieri, et al.
Human Mutation|January 1, 2008
Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of gliomaYanhong Liu, Keke Zhou, Haishi Zhang, et al.
Human Mutation|January 9, 2008
Patterns of missplicing caused by RB1 gene mutations in patients with retinoblastoma and association with phenotypic expressionKatherine Zhang, Inga Nowak, Diane Rushlow, et al.
Human Mutation|January 12, 2008
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)Steven Bentivegna, Jianbiao Zheng, Eugeni Namsaraev, et al.
Human Mutation|January 19, 2006
A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriersA Osorio, B Martínez-Delgado, M Pollán, et al.
Human Mutation|January 19, 2006
2005 Human Genome Variation Society Scientific MeetingWilliam S Oetting
Human Mutation|January 1, 1995
Identification of a one-basepair deletion in exon 6 of the dystrophin geneG N Kavaslar, M Telatar, P Serdaroglu, et al.
Human Mutation|January 1, 1995
An Alu1- polymorphism in the HEXA gene is common in Ashkenazi and Sephardic Jews, Israeli Arabs, and French Canadians of Quebec and northern New EnglandJ Grinshpun, R Khosravi, L Peleg, et al.
Pageof 655

Showing results (831-840 of 6,545) with videos related to

Sort By:
Pageof 655
Human Mutation|December 7, 2007
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based arrayTeresita Díaz de Ståhl, Johanna Sandgren, Arkadiusz Piotrowski, et al.
Human Mutation|December 7, 2007
Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related diseaseAlessandro Pecci, Emanuele Panza, Núria Pujol-Moix, et al.
Human Mutation|February 14, 2006
Study of four genes belonging to the folate pathway: transcobalamin 2 is involved in the onset of non-syndromic cleft lip with or without cleft palateMarcella Martinelli, Luca Scapoli, Annalisa Palmieri, et al.
Human Mutation|January 1, 2008
Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of gliomaYanhong Liu, Keke Zhou, Haishi Zhang, et al.
Human Mutation|January 9, 2008
Patterns of missplicing caused by RB1 gene mutations in patients with retinoblastoma and association with phenotypic expressionKatherine Zhang, Inga Nowak, Diane Rushlow, et al.
Human Mutation|January 12, 2008
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)Steven Bentivegna, Jianbiao Zheng, Eugeni Namsaraev, et al.
Human Mutation|January 19, 2006
A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriersA Osorio, B Martínez-Delgado, M Pollán, et al.
Human Mutation|January 19, 2006
2005 Human Genome Variation Society Scientific MeetingWilliam S Oetting
Human Mutation|January 1, 1995
Identification of a one-basepair deletion in exon 6 of the dystrophin geneG N Kavaslar, M Telatar, P Serdaroglu, et al.
Human Mutation|January 1, 1995
An Alu1- polymorphism in the HEXA gene is common in Ashkenazi and Sephardic Jews, Israeli Arabs, and French Canadians of Quebec and northern New EnglandJ Grinshpun, R Khosravi, L Peleg, et al.
Pageof 655