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D Walsh

Showing results (771-780 of 946) with videos related to

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American Journal of Medical Genetics|April 9, 1996
Irish study on high-density schizophrenia families: field methods and power to detect linkageK S Kendler, F A O'Neill, J Burke, et al.
Plos One|February 26, 2013
Physical and emotional health problems experienced by youth engaged in physical fighting and weapon carryingSophie D Walsh, Michal Molcho, Wendy Craig, et al.
The Journal of Organic Chemistry|July 20, 2002
Synthesis of [n]- and [n.n]cyclophanes by using Suzuki-Miyaura couplingBeverly B Smith, Darron E Hill, T Ashton Cropp, et al.
Journal of the Air & Waste Management Association (1995)|August 12, 2000
Use of a continuous nephelometer to measure personal exposure to particles during the U.S. Environmental Protection Agency Baltimore and Fresno Panel studiesC Howard-Reed, A W Rea, M J Zufall, et al.
Familial Cancer|April 10, 2025
Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylationJihoon E Joo, Khalid Mahmood, Mark Clendenning, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 22, 2006
Catechol-O-methyltransferase and the clinical features of psychosisJ L McClay, A Fanous, E J C G van den Oord, et al.
AEM Education and Training|October 11, 2023
Implementing ultrasound-guided nerve blocks in the emergency department: A low-cost, low-fidelity training approachCarrie D Walsh, Irene W Y Ma, Andrew J Eyre, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2014
Vaccinating captive chimpanzees to save wild chimpanzeesKelly L Warfield, Jason E Goetzmann, Julia E Biggins, et al.
Familial Cancer|March 2, 2011
Mutation deep within an intron of MSH2 causes Lynch syndromeMark Clendenning, Daniel D Buchanan, Michael D Walsh, et al.
Clinical and Experimental Dermatology|November 22, 2021
Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1)D Wen, D L Balacco, A Bardhan, et al.
Pageof 95

Showing results (771-780 of 946) with videos related to

Sort By:
Pageof 95
American Journal of Medical Genetics|April 9, 1996
Irish study on high-density schizophrenia families: field methods and power to detect linkageK S Kendler, F A O'Neill, J Burke, et al.
Plos One|February 26, 2013
Physical and emotional health problems experienced by youth engaged in physical fighting and weapon carryingSophie D Walsh, Michal Molcho, Wendy Craig, et al.
The Journal of Organic Chemistry|July 20, 2002
Synthesis of [n]- and [n.n]cyclophanes by using Suzuki-Miyaura couplingBeverly B Smith, Darron E Hill, T Ashton Cropp, et al.
Journal of the Air & Waste Management Association (1995)|August 12, 2000
Use of a continuous nephelometer to measure personal exposure to particles during the U.S. Environmental Protection Agency Baltimore and Fresno Panel studiesC Howard-Reed, A W Rea, M J Zufall, et al.
Familial Cancer|April 10, 2025
Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylationJihoon E Joo, Khalid Mahmood, Mark Clendenning, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 22, 2006
Catechol-O-methyltransferase and the clinical features of psychosisJ L McClay, A Fanous, E J C G van den Oord, et al.
AEM Education and Training|October 11, 2023
Implementing ultrasound-guided nerve blocks in the emergency department: A low-cost, low-fidelity training approachCarrie D Walsh, Irene W Y Ma, Andrew J Eyre, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2014
Vaccinating captive chimpanzees to save wild chimpanzeesKelly L Warfield, Jason E Goetzmann, Julia E Biggins, et al.
Familial Cancer|March 2, 2011
Mutation deep within an intron of MSH2 causes Lynch syndromeMark Clendenning, Daniel D Buchanan, Michael D Walsh, et al.
Clinical and Experimental Dermatology|November 22, 2021
Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1)D Wen, D L Balacco, A Bardhan, et al.
Pageof 95