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American Journal of Medical Genetics
|
February 15, 1992
Linkage analysis in juvenile neuronal ceroid lipofuscinosis
J 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 gene
B 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 loci
C 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 11
Y 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 16
M 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 locus
C 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 mellitus
J Hager, L Hansen, C Vaisse, et al.
Human Genetics
|
December 1, 1988
Linkage studies in X-linked Alport's syndrome
S 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 perspectives
R White, M Leppert, P O'Connell, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 97) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics
|
February 15, 1992
Linkage analysis in juvenile neuronal ceroid lipofuscinosis
J 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 gene
B 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 loci
C 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 11
Y 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 16
M 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 locus
C 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 mellitus
J Hager, L Hansen, C Vaisse, et al.
Human Genetics
|
December 1, 1988
Linkage studies in X-linked Alport's syndrome
S 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 perspectives
R White, M Leppert, P O'Connell, et al.
Page
of 10