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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 breakpoints
P 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 17p
E 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 chromosome
P 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 syndrome
J 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 paraplegia
F Cambi, X M Tang, P Cordray, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1986
Highly polymorphic RFLP probes as diagnostic tools
H 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 markers
J 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 achondroplasia
S M Pulst, T Pribyl, D F Barker, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 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 breakpoints
P 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 17p
E 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 chromosome
P 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 syndrome
J 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 paraplegia
F Cambi, X M Tang, P Cordray, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1986
Highly polymorphic RFLP probes as diagnostic tools
H 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 markers
J 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 achondroplasia
S M Pulst, T Pribyl, D F Barker, et al.
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of 8