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C Morton

Showing results (701-710 of 853) with videos related to

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Cytogenetics and Cell Genetics|April 18, 2001
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14G M Caldwell, R L Eddy, C D Day, et al.
BMC Genomics|June 5, 2024
Targeted insertion of conditional expression cassettes into the mouse genome using the modified i-PITTHiromi Miura, Ayaka Nakamura, Aki Kurosaki, et al.
Scientific Data|November 29, 2025
Landscape fire emissions from the 5<sup>th</sup> version of the Global Fire Emissions Database (GFED5)Guido R van der Werf, James T Randerson, Dave van Wees, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Medical Care|December 22, 1999
The impact of competing subsistence needs and barriers on access to medical care for persons with human immunodeficiency virus receiving care in the United StatesW E Cunningham, R M Andersen, M H Katz, et al.
JAMA|July 1, 1999
Variations in the care of HIV-infected adults in the United States: results from the HIV Cost and Services Utilization StudyM F Shapiro, S C Morton, D F McCaffrey, et al.
American Journal of Obstetrics and Gynecology|January 30, 2008
The impact of race as a risk factor for symptom severity and age at diagnosis of uterine leiomyomata among affected sistersKaren L Huyck, Carolien I M Panhuysen, Karen T Cuenco, et al.
European Heart Journal|August 1, 2014
The effect of interleukin-1 receptor antagonist therapy on markers of inflammation in non-ST elevation acute coronary syndromes: the MRC-ILA Heart StudyAllison C Morton, Alexander M K Rothman, John P Greenwood, et al.
Nature Genetics|February 26, 2013
Using population admixture to help complete maps of the human genomeGiulio Genovese, Robert E Handsaker, Heng Li, et al.
Genomics|October 14, 2000
SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseasesC N Adra, J L Donato, R Badovinac, et al.
Pageof 86

Showing results (701-710 of 853) with videos related to

Sort By:
Pageof 86
Cytogenetics and Cell Genetics|April 18, 2001
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14G M Caldwell, R L Eddy, C D Day, et al.
BMC Genomics|June 5, 2024
Targeted insertion of conditional expression cassettes into the mouse genome using the modified i-PITTHiromi Miura, Ayaka Nakamura, Aki Kurosaki, et al.
Scientific Data|November 29, 2025
Landscape fire emissions from the 5<sup>th</sup> version of the Global Fire Emissions Database (GFED5)Guido R van der Werf, James T Randerson, Dave van Wees, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Medical Care|December 22, 1999
The impact of competing subsistence needs and barriers on access to medical care for persons with human immunodeficiency virus receiving care in the United StatesW E Cunningham, R M Andersen, M H Katz, et al.
JAMA|July 1, 1999
Variations in the care of HIV-infected adults in the United States: results from the HIV Cost and Services Utilization StudyM F Shapiro, S C Morton, D F McCaffrey, et al.
American Journal of Obstetrics and Gynecology|January 30, 2008
The impact of race as a risk factor for symptom severity and age at diagnosis of uterine leiomyomata among affected sistersKaren L Huyck, Carolien I M Panhuysen, Karen T Cuenco, et al.
European Heart Journal|August 1, 2014
The effect of interleukin-1 receptor antagonist therapy on markers of inflammation in non-ST elevation acute coronary syndromes: the MRC-ILA Heart StudyAllison C Morton, Alexander M K Rothman, John P Greenwood, et al.
Nature Genetics|February 26, 2013
Using population admixture to help complete maps of the human genomeGiulio Genovese, Robert E Handsaker, Heng Li, et al.
Genomics|October 14, 2000
SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseasesC N Adra, J L Donato, R Badovinac, et al.
Pageof 86