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D H Ledbetter

Showing results (101-110 of 251) with videos related to

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Genes & Development|April 1, 1995
Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome regionP H Gunaratne, M Nakao, D H Ledbetter, et al.
American Journal of Human Genetics|October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridizationA Kuwano, S A Ledbetter, W B Dobyns, et al.
American Journal of Medical Genetics|December 1, 1987
Duplication of proximal 15q as a cause of Prader-Willi syndromeA L Pettigrew, S M Gollin, F Greenberg, et al.
Human Molecular Genetics|February 1, 1994
Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E)M Nakao, J S Sutcliffe, B Durtschi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1987
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationR L Nussbaum, J G Lesko, R A Lewis, et al.
Human Genetics|June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1N Morrison, J P Goddard, D H Ledbetter, et al.
The Journal of Pediatrics|May 1, 1993
Wilms tumor in a patient with Prader-Willi syndromeM J Coppes, H Sohl, I E Teshima, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instabilityD H Ledbetter, V M Riccardi, W W Au, et al.
American Journal of Human Genetics|April 1, 1990
Five polymorphic microsatellite VNTRs on the human X chromosomeJ A Luty, Z Guo, H F Willard, et al.
American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.
Pageof 26

Showing results (101-110 of 251) with videos related to

Sort By:
Pageof 26
Genes & Development|April 1, 1995
Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome regionP H Gunaratne, M Nakao, D H Ledbetter, et al.
American Journal of Human Genetics|October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridizationA Kuwano, S A Ledbetter, W B Dobyns, et al.
American Journal of Medical Genetics|December 1, 1987
Duplication of proximal 15q as a cause of Prader-Willi syndromeA L Pettigrew, S M Gollin, F Greenberg, et al.
Human Molecular Genetics|February 1, 1994
Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E)M Nakao, J S Sutcliffe, B Durtschi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1987
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationR L Nussbaum, J G Lesko, R A Lewis, et al.
Human Genetics|June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1N Morrison, J P Goddard, D H Ledbetter, et al.
The Journal of Pediatrics|May 1, 1993
Wilms tumor in a patient with Prader-Willi syndromeM J Coppes, H Sohl, I E Teshima, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instabilityD H Ledbetter, V M Riccardi, W W Au, et al.
American Journal of Human Genetics|April 1, 1990
Five polymorphic microsatellite VNTRs on the human X chromosomeJ A Luty, Z Guo, H F Willard, et al.
American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.
Pageof 26