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D F Barker

Showing results (21-30 of 71) with videos related to

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Nucleic Acids Research|March 25, 1992
Dinucleotide repeat polymorphism at the DXS441 locusK T Ram, D F Barker, J M Puck
Genetics|November 1, 1978
Properties of the translocatable tetracycline-resistance element Tn10 in Escherichia coli and bacteriophage lambdaN Kleckner, D F Barker, D G Ross, et al.
Human Molecular Genetics|April 1, 1993
Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplicationV V Ionasescu, R Ionasescu, C Searby, et al.
American Journal of Medical Genetics|February 27, 2001
Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCPD F Barker, J C Denison, C L Atkin, et al.
Contributions to Nephrology|January 1, 1996
Application of linked markers for genetic diagnosis of Alport syndromeD F Barker, C L Atkin, M C Gregory, et al.
Nucleic Acids Research|January 25, 1989
Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22)E C Wright, P R Fain, D F Barker, et al.
Nucleic Acids Research|January 25, 1989
A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22)E C Wright, P R Fain, D F Barker, et al.
American Journal of Human Genetics|June 19, 1998
Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosomeA K Naumova, M Leppert, D F Barker, et al.
Human Genetics|May 1, 1997
Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677QD F Barker, J C Denison, C L Atkin, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|March 25, 1992
Dinucleotide repeat polymorphism at the DXS441 locusK T Ram, D F Barker, J M Puck
Genetics|November 1, 1978
Properties of the translocatable tetracycline-resistance element Tn10 in Escherichia coli and bacteriophage lambdaN Kleckner, D F Barker, D G Ross, et al.
Human Molecular Genetics|April 1, 1993
Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplicationV V Ionasescu, R Ionasescu, C Searby, et al.
American Journal of Medical Genetics|February 27, 2001
Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCPD F Barker, J C Denison, C L Atkin, et al.
Contributions to Nephrology|January 1, 1996
Application of linked markers for genetic diagnosis of Alport syndromeD F Barker, C L Atkin, M C Gregory, et al.
Nucleic Acids Research|January 25, 1989
Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22)E C Wright, P R Fain, D F Barker, et al.
Nucleic Acids Research|January 25, 1989
A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22)E C Wright, P R Fain, D F Barker, et al.
American Journal of Human Genetics|June 19, 1998
Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosomeA K Naumova, M Leppert, D F Barker, et al.
Human Genetics|May 1, 1997
Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677QD F Barker, J C Denison, C L Atkin, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
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