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H Ledbetter

Showing results (251-260 of 388) with videos related to

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Science (New York, N.Y.)|June 2, 1989
Two NF1 translocations map within a 600-kilobase segment of 17q11.2P O'Connell, R Leach, R M Cawthon, et al.
Genomics|September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
The American Journal of Psychiatry|December 7, 2022
Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System PopulationHermela Shimelis, Matthew T Oetjens, Lauren K Walsh, et al.
American Journal of Medical Genetics|February 22, 2002
Mutation screening and transmission disequilibrium study of ATP10C in autismSoo-Jeong Kim, Laura B K Herzing, Jeremy Veenstra-VanderWeele, et al.
The Journal of the Acoustical Society of America|October 2, 2007
Alpha-plutonium's polycrystalline elastic moduli over its full temperature rangeA Migliori, C Pantea, H Ledbetter, et al.
Somatic Cell and Molecular Genetics|July 1, 1987
Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localizationG I Liou, S L Fong, J Gosden, et al.
American Journal of Obstetrics and Gynecology|February 1, 1990
Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative studyD H Ledbetter, A O Martin, Y Verlinsky, et al.
Nature Communications|October 15, 2024
A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism riskAlexander S F Berry, Brenda M Finucane, Scott M Myers, et al.
American Journal of Human Genetics|November 1, 1992
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGMR A Bascom, J García-Heras, C L Hsieh, et al.
Genomics|December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN geneA Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Pageof 39

Showing results (251-260 of 388) with videos related to

Sort By:
Pageof 39
Science (New York, N.Y.)|June 2, 1989
Two NF1 translocations map within a 600-kilobase segment of 17q11.2P O'Connell, R Leach, R M Cawthon, et al.
Genomics|September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
The American Journal of Psychiatry|December 7, 2022
Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System PopulationHermela Shimelis, Matthew T Oetjens, Lauren K Walsh, et al.
American Journal of Medical Genetics|February 22, 2002
Mutation screening and transmission disequilibrium study of ATP10C in autismSoo-Jeong Kim, Laura B K Herzing, Jeremy Veenstra-VanderWeele, et al.
The Journal of the Acoustical Society of America|October 2, 2007
Alpha-plutonium's polycrystalline elastic moduli over its full temperature rangeA Migliori, C Pantea, H Ledbetter, et al.
Somatic Cell and Molecular Genetics|July 1, 1987
Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localizationG I Liou, S L Fong, J Gosden, et al.
American Journal of Obstetrics and Gynecology|February 1, 1990
Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative studyD H Ledbetter, A O Martin, Y Verlinsky, et al.
Nature Communications|October 15, 2024
A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism riskAlexander S F Berry, Brenda M Finucane, Scott M Myers, et al.
American Journal of Human Genetics|November 1, 1992
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGMR A Bascom, J García-Heras, C L Hsieh, et al.
Genomics|December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN geneA Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Pageof 39