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American Journal of Human Genetics
|
October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2
M Horwitz, K F Benson, F Q Li, et al.
Cancer Research
|
March 1, 1996
Three secretory phospholipase A(2) genes that map to human chromosome 1P35-36 are not mutated in individuals with attenuated adenomatous polyposis coli
L N Spirio, W Kutchera, M V Winstead, et al.
Genomics
|
August 1, 1994
Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36
Y R Su, C A Klanke, T W Houseal, et al.
Annals of Epidemiology
|
August 30, 2000
NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network
R R Williams, D C Rao, R C Ellison, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1996
Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains
H Heath, S Odelberg, C E Jackson, et al.
The American Journal of Pathology
|
April 6, 2001
Inverse relationship between microsatellite instability and K-ras and p53 gene alterations in colon cancer
W S Samowitz, J A Holden, K Curtin, et al.
Genes and Immunity
|
December 14, 2007
Variants in the 5q31 cytokine gene cluster are associated with psoriasis
M Chang, Y Li, C Yan, et al.
Genes and Immunity
|
July 25, 2008
Detailed genetic characterization of the interleukin-23 receptor in psoriasis
V E Garcia, M Chang, R Brandon, et al.
Neuroimage. Clinical
|
February 1, 2017
Multivariate characterization of white matter heterogeneity in autism spectrum disorder
D C Dean, N Lange, B G Travers, et al.
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of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
American Journal of Human Genetics
|
October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2
M Horwitz, K F Benson, F Q Li, et al.
Cancer Research
|
March 1, 1996
Three secretory phospholipase A(2) genes that map to human chromosome 1P35-36 are not mutated in individuals with attenuated adenomatous polyposis coli
L N Spirio, W Kutchera, M V Winstead, et al.
Genomics
|
August 1, 1994
Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36
Y R Su, C A Klanke, T W Houseal, et al.
Annals of Epidemiology
|
August 30, 2000
NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network
R R Williams, D C Rao, R C Ellison, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1996
Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains
H Heath, S Odelberg, C E Jackson, et al.
The American Journal of Pathology
|
April 6, 2001
Inverse relationship between microsatellite instability and K-ras and p53 gene alterations in colon cancer
W S Samowitz, J A Holden, K Curtin, et al.
Genes and Immunity
|
December 14, 2007
Variants in the 5q31 cytokine gene cluster are associated with psoriasis
M Chang, Y Li, C Yan, et al.
Genes and Immunity
|
July 25, 2008
Detailed genetic characterization of the interleukin-23 receptor in psoriasis
V E Garcia, M Chang, R Brandon, et al.
Neuroimage. Clinical
|
February 1, 2017
Multivariate characterization of white matter heterogeneity in autism spectrum disorder
D C Dean, N Lange, B G Travers, et al.
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of 5