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Nucleic Acids Research
|
March 25, 1992
Dinucleotide repeat polymorphism at the DXS441 locus
K 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 lambda
N 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-duplication
V 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-SSCP
D 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 syndrome
D 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 chromosome
A 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 R1677Q
D 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.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Nucleic Acids Research
|
March 25, 1992
Dinucleotide repeat polymorphism at the DXS441 locus
K 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 lambda
N 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-duplication
V 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-SSCP
D 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 syndrome
D 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 chromosome
A 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 R1677Q
D 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.
Page
of 8