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D F Barker

Showing results (31-40 of 71) with videos related to

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American Journal of Human Genetics|January 1, 1989
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpointsP R Fain, E Wright, H F Willard, et al.
Nucleic Acids Research|January 25, 1989
A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12)D F Barker, P R Fain, E C Wright, et al.
Nucleic Acids Research|January 25, 1989
MspI RFLP at CRYB1 locus (17q11.2----17q12)D F Barker, P R Fain, E C Wright, et al.
Genomics|May 1, 1990
A genetic map of human chromosome 17pE C Wright, D E Goldgar, P R Fain, et al.
Genomics|December 1, 1991
Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosomeP R Fain, J A Luty, Z Guo, et al.
Genomics|January 1, 1991
Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndromeJ Zhou, D F Barker, S L Hostikka, et al.
Neurology|April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegiaF Cambi, X M Tang, P Cordray, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Highly polymorphic RFLP probes as diagnostic toolsH Donis-Keller, D F Barker, R G Knowlton, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markersJ N Dietz-Band, A E Turco, H F Willard, et al.
American Journal of Medical Genetics|July 1, 1991
Molecular analysis of a patient with neurofibromatosis 1 and achondroplasiaS M Pulst, T Pribyl, D F Barker, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|January 1, 1989
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpointsP R Fain, E Wright, H F Willard, et al.
Nucleic Acids Research|January 25, 1989
A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12)D F Barker, P R Fain, E C Wright, et al.
Nucleic Acids Research|January 25, 1989
MspI RFLP at CRYB1 locus (17q11.2----17q12)D F Barker, P R Fain, E C Wright, et al.
Genomics|May 1, 1990
A genetic map of human chromosome 17pE C Wright, D E Goldgar, P R Fain, et al.
Genomics|December 1, 1991
Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosomeP R Fain, J A Luty, Z Guo, et al.
Genomics|January 1, 1991
Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndromeJ Zhou, D F Barker, S L Hostikka, et al.
Neurology|April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegiaF Cambi, X M Tang, P Cordray, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Highly polymorphic RFLP probes as diagnostic toolsH Donis-Keller, D F Barker, R G Knowlton, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markersJ N Dietz-Band, A E Turco, H F Willard, et al.
American Journal of Medical Genetics|July 1, 1991
Molecular analysis of a patient with neurofibromatosis 1 and achondroplasiaS M Pulst, T Pribyl, D F Barker, et al.
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