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L M Brzustowicz

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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 6pL 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 17M 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-->q13.3L E Bernard, J D McPherson, J J Wasmuth, et al.
American Journal of Human Genetics|September 16, 1999
Linkage of familial schizophrenia to chromosome 13q32L 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 impairmentP Tallal, L S Hirsch, T Realpe-Bonilla, et al.
Genetic Epidemiology|January 1, 1997
False positive rates in a genomic screen for complex quantitative traitsW 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 lymphoblastsL 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 locusP 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 5q13L 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 atrophyL M Brzustowicz, B A Allitto, D Matseoane, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 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 6pL 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 17M 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-->q13.3L E Bernard, J D McPherson, J J Wasmuth, et al.
American Journal of Human Genetics|September 16, 1999
Linkage of familial schizophrenia to chromosome 13q32L 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 impairmentP Tallal, L S Hirsch, T Realpe-Bonilla, et al.
Genetic Epidemiology|January 1, 1997
False positive rates in a genomic screen for complex quantitative traitsW 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 lymphoblastsL 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 locusP 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 5q13L 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 atrophyL M Brzustowicz, B A Allitto, D Matseoane, et al.
Pageof 4