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American Journal of Human Genetics
|
December 18, 1997
Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p
L M Brzustowicz, W G Honer, E W Chow, et al.
Human Heredity
|
October 5, 2006
A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17
M W Logue, L M Brzustowicz, A S Bassett, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Linkage mapping detects two secondary microdeletions in cell hybrid HHW1064, used to isolate DNA probes from within 5q11.2-->q13.3
L E Bernard, J D McPherson, J J Wasmuth, et al.
American Journal of Human Genetics
|
September 16, 1999
Linkage of familial schizophrenia to chromosome 13q32
L M Brzustowicz, W G Honer, E W Chow, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
November 16, 2001
Familial aggregation in specific language impairment
P Tallal, L S Hirsch, T Realpe-Bonilla, et al.
Genetic Epidemiology
|
January 1, 1997
False positive rates in a genomic screen for complex quantitative traits
W K Scott, M C Speer, S M Leal, et al.
Hypertension (Dallas, Tex. : 1979)
|
January 1, 1997
Linkage analysis using platelet-activating factor Ca2+ response in transformed lymphoblasts
L M Brzustowicz, J P Gardner, L Hopp, et al.
Neurology
|
September 1, 1991
Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus
P W Kleyn, L M Brzustowicz, K C Wilhelmsen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1991
Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13
L L Lien, F M Boyce, P Kleyn, et al.
American Journal of Human Genetics
|
March 1, 1994
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy
L M Brzustowicz, B A Allitto, D Matseoane, et al.
Page
of 4
Search research articles
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Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
American Journal of Human Genetics
|
December 18, 1997
Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p
L M Brzustowicz, W G Honer, E W Chow, et al.
Human Heredity
|
October 5, 2006
A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17
M W Logue, L M Brzustowicz, A S Bassett, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Linkage mapping detects two secondary microdeletions in cell hybrid HHW1064, used to isolate DNA probes from within 5q11.2-->q13.3
L E Bernard, J D McPherson, J J Wasmuth, et al.
American Journal of Human Genetics
|
September 16, 1999
Linkage of familial schizophrenia to chromosome 13q32
L M Brzustowicz, W G Honer, E W Chow, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
November 16, 2001
Familial aggregation in specific language impairment
P Tallal, L S Hirsch, T Realpe-Bonilla, et al.
Genetic Epidemiology
|
January 1, 1997
False positive rates in a genomic screen for complex quantitative traits
W K Scott, M C Speer, S M Leal, et al.
Hypertension (Dallas, Tex. : 1979)
|
January 1, 1997
Linkage analysis using platelet-activating factor Ca2+ response in transformed lymphoblasts
L M Brzustowicz, J P Gardner, L Hopp, et al.
Neurology
|
September 1, 1991
Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus
P W Kleyn, L M Brzustowicz, K C Wilhelmsen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1991
Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13
L L Lien, F M Boyce, P Kleyn, et al.
American Journal of Human Genetics
|
March 1, 1994
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy
L M Brzustowicz, B A Allitto, D Matseoane, et al.
Page
of 4