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H Ledbetter

Showing results (131-140 of 388) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2025
Reconciling competencies in undergraduate medical genetics education: APHMG versus PCME competenciesRachel D Burnside, Megan Boothe, David H Ledbetter, et al.
American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.
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.
Physical Review Letters|October 4, 2005
Complete elastic tensor through the first-order transformation in U2Rh3Si5R G Leisure, S Kern, F R Drymiotis, 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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2025
Apples, Oranges, and Biobanks: Ascertainment Bias in Population-Based Studies of Neurodevelopmental Psychiatric DisordersBrenda M Finucane, Scott M Myers, David H Ledbetter, et al.
Nucleic Acids Research|September 12, 1988
Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]D C Rich, C M Witkowski, K M Summers, et al.
Nature Communications|October 27, 2019
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disordersM T Oetjens, M A Kelly, A C Sturm, et al.
Pageof 39

Showing results (131-140 of 388) with videos related to

Sort By:
Pageof 39
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2025
Reconciling competencies in undergraduate medical genetics education: APHMG versus PCME competenciesRachel D Burnside, Megan Boothe, David H Ledbetter, et al.
American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.
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.
Physical Review Letters|October 4, 2005
Complete elastic tensor through the first-order transformation in U2Rh3Si5R G Leisure, S Kern, F R Drymiotis, 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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2025
Apples, Oranges, and Biobanks: Ascertainment Bias in Population-Based Studies of Neurodevelopmental Psychiatric DisordersBrenda M Finucane, Scott M Myers, David H Ledbetter, et al.
Nucleic Acids Research|September 12, 1988
Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]D C Rich, C M Witkowski, K M Summers, et al.
Nature Communications|October 27, 2019
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disordersM T Oetjens, M A Kelly, A C Sturm, et al.
Pageof 39