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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-->p14
G 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-PITT
Hiromi 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 States
W 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 Study
M 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 sisters
Karen 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 Study
Allison 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 genome
Giulio 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 diseases
C N Adra, J L Donato, R Badovinac, et al.
Page
of 86
Search research articles
Search
Showing results (701-710 of 853) with videos related to
Sort By:
Page
of 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-->p14
G 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-PITT
Hiromi 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 States
W 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 Study
M 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 sisters
Karen 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 Study
Allison 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 genome
Giulio 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 diseases
C N Adra, J L Donato, R Badovinac, et al.
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of 86