Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D F Barker

Showing results (51-60 of 71) with videos related to

Pageof 8
Sort By:
American Journal of Medical Genetics|April 1, 1992
MRX8: an X-linked mental retardation condition with linkage to Xq21C E Schwartz, M May, T Huang, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Genomics|December 1, 1987
Genetic analysis of NF1: identification of close flanking markers on chromosome 17P R Fain, D F Barker, D E Goldgar, et al.
Genomics|February 1, 1993
Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22O Parolini, J F Hejtmancik, R C Allen, et al.
Genetic Epidemiology|January 1, 1996
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotypeD F Barker, E R Almeida, G Casey, et al.
Nature|February 8, 1990
Paternal origin of new mutations in von Recklinghausen neurofibromatosisD Jadayel, P Fain, M Upadhyaya, et al.
Genetic Epidemiology|January 1, 1989
Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 dataN J Cox, K J Gogolin, V J Horvath, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome regionD H Ledbetter, S A Ledbetter, P vanTuinen, et al.
American Journal of Human Genetics|January 1, 1988
Identification of more than 500 RFLPs by screening random genomic clonesJ W Schumm, R G Knowlton, J C Braman, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|April 1, 1992
MRX8: an X-linked mental retardation condition with linkage to Xq21C E Schwartz, M May, T Huang, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Genomics|December 1, 1987
Genetic analysis of NF1: identification of close flanking markers on chromosome 17P R Fain, D F Barker, D E Goldgar, et al.
Genomics|February 1, 1993
Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22O Parolini, J F Hejtmancik, R C Allen, et al.
Genetic Epidemiology|January 1, 1996
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotypeD F Barker, E R Almeida, G Casey, et al.
Nature|February 8, 1990
Paternal origin of new mutations in von Recklinghausen neurofibromatosisD Jadayel, P Fain, M Upadhyaya, et al.
Genetic Epidemiology|January 1, 1989
Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 dataN J Cox, K J Gogolin, V J Horvath, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome regionD H Ledbetter, S A Ledbetter, P vanTuinen, et al.
American Journal of Human Genetics|January 1, 1988
Identification of more than 500 RFLPs by screening random genomic clonesJ W Schumm, R G Knowlton, J C Braman, et al.
Pageof 8