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C Julier

Showing results (61-70 of 97) with videos related to

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American Journal of Medical Genetics|February 15, 1992
Linkage analysis in juvenile neuronal ceroid lipofuscinosisJ L Haines, W L Yan, R M Boustany, et al.
Human Molecular Genetics|September 16, 1998
Measured haplotype analysis of the angiotensin-I converting enzyme geneB Keavney, C A McKenzie, J M Connell, et al.
American Journal of Human Genetics|December 1, 1995
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait lociC A McKenzie, C Julier, T Forrester, et al.
American Journal of Human Genetics|May 1, 1989
Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11Y Nakamura, C Larsson, C Julier, et al.
Journal of Medical Genetics|May 3, 2005
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?E Cadet, D Capron, M Gallet, et al.
Genomics|October 1, 1990
Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16M Gardiner, A Sandford, M Deadman, et al.
Genomics|July 1, 1993
A radiation hybrid map of human chromosome 11q22-q23 containing the ataxia-telangiectasia disease locusC W Richard, D R Cox, L Kapp, et al.
Nature Genetics|March 1, 1995
A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitusJ Hager, L Hansen, C Vaisse, et al.
Human Genetics|December 1, 1988
Linkage studies in X-linked Alport's syndromeS Szpiro-Tapia, G Bobrie, M Guilloud-Bataille, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Construction of human genetic linkage maps: I. Progress and perspectivesR White, M Leppert, P O'Connell, et al.
Pageof 10

Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics|February 15, 1992
Linkage analysis in juvenile neuronal ceroid lipofuscinosisJ L Haines, W L Yan, R M Boustany, et al.
Human Molecular Genetics|September 16, 1998
Measured haplotype analysis of the angiotensin-I converting enzyme geneB Keavney, C A McKenzie, J M Connell, et al.
American Journal of Human Genetics|December 1, 1995
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait lociC A McKenzie, C Julier, T Forrester, et al.
American Journal of Human Genetics|May 1, 1989
Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11Y Nakamura, C Larsson, C Julier, et al.
Journal of Medical Genetics|May 3, 2005
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?E Cadet, D Capron, M Gallet, et al.
Genomics|October 1, 1990
Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16M Gardiner, A Sandford, M Deadman, et al.
Genomics|July 1, 1993
A radiation hybrid map of human chromosome 11q22-q23 containing the ataxia-telangiectasia disease locusC W Richard, D R Cox, L Kapp, et al.
Nature Genetics|March 1, 1995
A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitusJ Hager, L Hansen, C Vaisse, et al.
Human Genetics|December 1, 1988
Linkage studies in X-linked Alport's syndromeS Szpiro-Tapia, G Bobrie, M Guilloud-Bataille, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Construction of human genetic linkage maps: I. Progress and perspectivesR White, M Leppert, P O'Connell, et al.
Pageof 10