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J C Murray

Showing results (141-150 of 328) with videos related to

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Clinical Genetics|June 28, 2007
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palateF E Abidi, M G Miano, J C Murray, et al.
Nucleic Acids Research|August 25, 1988
RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19H H Ardinger, R H Ardinger, G I Bell, et al.
European Geriatric Medicine|April 17, 2020
The identification of probable sarcopenia in early old age based on the SARC-F tool and clinical suspicion: findings from the 1946 British birth cohortR M Dodds, J C Murray, S M Robinson, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Localization of two new DNA markers on the linkage map of human chromosome 6qB C Byth, D R Love, J C Murray, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemiaJ C Murray, C M Demopulos, R M Lawn, et al.
Nucleic Acids Research|March 25, 1988
A TaqI RFLP demonstrated for pIBS17 [D4S123], a single copy sequence on chromosome 4L D Berdahl, R F Smith, J C Murray, et al.
The Journal of Investigative Dermatology|July 1, 1978
Connective tissue structure: cell binding to collagenH K Kleinman, J C Murray, E B McGoodwin, et al.
Neurology|February 1, 1987
Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markersP F Chance, J C Murray, T D Bird, et al.
Journal of the American Academy of Dermatology|May 1, 1992
Generalized papular xanthomatosis in mycosis fungoidesB S Darwin, A J Herzberg, J C Murray, et al.
Genomics|May 1, 1995
Genomic organization of the human osteopontin gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type IIA H Crosby, S J Edwards, J C Murray, et al.
Pageof 33

Showing results (141-150 of 328) with videos related to

Sort By:
Pageof 33
Clinical Genetics|June 28, 2007
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palateF E Abidi, M G Miano, J C Murray, et al.
Nucleic Acids Research|August 25, 1988
RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19H H Ardinger, R H Ardinger, G I Bell, et al.
European Geriatric Medicine|April 17, 2020
The identification of probable sarcopenia in early old age based on the SARC-F tool and clinical suspicion: findings from the 1946 British birth cohortR M Dodds, J C Murray, S M Robinson, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Localization of two new DNA markers on the linkage map of human chromosome 6qB C Byth, D R Love, J C Murray, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemiaJ C Murray, C M Demopulos, R M Lawn, et al.
Nucleic Acids Research|March 25, 1988
A TaqI RFLP demonstrated for pIBS17 [D4S123], a single copy sequence on chromosome 4L D Berdahl, R F Smith, J C Murray, et al.
The Journal of Investigative Dermatology|July 1, 1978
Connective tissue structure: cell binding to collagenH K Kleinman, J C Murray, E B McGoodwin, et al.
Neurology|February 1, 1987
Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markersP F Chance, J C Murray, T D Bird, et al.
Journal of the American Academy of Dermatology|May 1, 1992
Generalized papular xanthomatosis in mycosis fungoidesB S Darwin, A J Herzberg, J C Murray, et al.
Genomics|May 1, 1995
Genomic organization of the human osteopontin gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type IIA H Crosby, S J Edwards, J C Murray, et al.
Pageof 33