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D F Barker

Showing results (41-50 of 71) with videos related to

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Gene|November 30, 1988
Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid librariesD W Bowden, H Müller-Kahle, T R Fulton, et al.
Kidney International|March 1, 1993
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndromeJ Zhou, M C Gregory, J M Hertz, et al.
Contributions to Nephrology|January 1, 1996
Alport syndrome--clinical phenotypes, incidence, and pathologyM C Gregory, D A Terreros, D F Barker, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets geneM J Econs, D F Barker, M C Speer, et al.
American Journal of Human Genetics|November 1, 1989
Refined physical and genetic mapping of the NF1 region on chromosome 17P R Fain, D E Goldgar, M R Wallace, et al.
American Journal of Human Genetics|March 21, 2000
X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3C L Bennett, R Yoshioka, H Kiyosawa, et al.
Nature Genetics|March 1, 1995
A 2D crossover-based map of the human X chromosome as a model for map integrationP R Fain, E N Kort, P F Chance, et al.
American Journal of Human Genetics|January 1, 1992
Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markersR V Lebo, E D Lynch, T D Bird, et al.
Genomics|October 1, 1991
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosomeR G Lafrenière, C J Brown, V E Powers, et al.
Journal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Gene|November 30, 1988
Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid librariesD W Bowden, H Müller-Kahle, T R Fulton, et al.
Kidney International|March 1, 1993
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndromeJ Zhou, M C Gregory, J M Hertz, et al.
Contributions to Nephrology|January 1, 1996
Alport syndrome--clinical phenotypes, incidence, and pathologyM C Gregory, D A Terreros, D F Barker, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets geneM J Econs, D F Barker, M C Speer, et al.
American Journal of Human Genetics|November 1, 1989
Refined physical and genetic mapping of the NF1 region on chromosome 17P R Fain, D E Goldgar, M R Wallace, et al.
American Journal of Human Genetics|March 21, 2000
X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3C L Bennett, R Yoshioka, H Kiyosawa, et al.
Nature Genetics|March 1, 1995
A 2D crossover-based map of the human X chromosome as a model for map integrationP R Fain, E N Kort, P F Chance, et al.
American Journal of Human Genetics|January 1, 1992
Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markersR V Lebo, E D Lynch, T D Bird, et al.
Genomics|October 1, 1991
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosomeR G Lafrenière, C J Brown, V E Powers, et al.
Journal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.
Pageof 8