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N H Chapman

Showing results (11-20 of 19) with videos related to

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British Journal of Haematology|May 8, 1999
Born to clot: the European burdenD C Rees, N H Chapman, M T Webster, et al.
Genetic Epidemiology|January 1, 1997
Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigreesJ Graham, N H Chapman, K A Goddard, et al.
Human Genetics|October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorderN H Chapman, R A Bernier, S J Webb, et al.
Molecular Psychiatry|March 9, 2005
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiencyW H Raskind, R P Igo, N H Chapman, et al.
Human Heredity|April 19, 2013
Identification of rare variants from exome sequence in a large pedigree with autismE E Marchani, N H Chapman, C Y K Cheung, et al.
Infection Control and Hospital Epidemiology|August 4, 1999
A randomized trial of 72- versus 24-hour intravenous tubing set changes in newborns receiving lipid therapyA G Matlow, I Kitai, H Kirpalani, et al.
Genetic Epidemiology|January 17, 2002
The importance of connections: joining components of the Hutterite pedigreeN H Chapman, A L Leutenegger, M D Badzioch, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Archives of Neurology|November 16, 2001
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of GuamP Poorkaj, D Tsuang, E Wijsman, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
British Journal of Haematology|May 8, 1999
Born to clot: the European burdenD C Rees, N H Chapman, M T Webster, et al.
Genetic Epidemiology|January 1, 1997
Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigreesJ Graham, N H Chapman, K A Goddard, et al.
Human Genetics|October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorderN H Chapman, R A Bernier, S J Webb, et al.
Molecular Psychiatry|March 9, 2005
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiencyW H Raskind, R P Igo, N H Chapman, et al.
Human Heredity|April 19, 2013
Identification of rare variants from exome sequence in a large pedigree with autismE E Marchani, N H Chapman, C Y K Cheung, et al.
Infection Control and Hospital Epidemiology|August 4, 1999
A randomized trial of 72- versus 24-hour intravenous tubing set changes in newborns receiving lipid therapyA G Matlow, I Kitai, H Kirpalani, et al.
Genetic Epidemiology|January 17, 2002
The importance of connections: joining components of the Hutterite pedigreeN H Chapman, A L Leutenegger, M D Badzioch, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Archives of Neurology|November 16, 2001
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of GuamP Poorkaj, D Tsuang, E Wijsman, et al.
Pageof 2