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Diabetes
|
December 4, 1998
Transmission of DQ haplotypes to patients with type 1 diabetes
E Kawasaki, J Noble, H Erlich, et al.
JAMA
|
September 11, 1981
Survival in hereditary breast and colon cancer
H T Lynch, W A Albano, J A Recabaren, et al.
Neurology
|
April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia
F Cambi, X M Tang, P Cordray, et al.
Cancer
|
June 1, 1981
Familial breast cancer and its recognition in an oncology clinic
H T Lynch, P R Fain, D Golgar, et al.
The New England Journal of Medicine
|
October 6, 1988
Linkage heterogeneity of autosomal dominant polycystic kidney disease
W J Kimberling, P R Fain, J B Kenyon, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1982
Genetic/epidemiological findings in a study of smoking-associated tumors
H T Lynch, P R Fain, W A Albano, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets gene
M J Econs, D F Barker, M C Speer, et al.
Human Heredity
|
November 14, 1998
No evidence for linkage of a novel CA repeat polymorphism for apoptosis antigen 1 (APO-1 or fas) with type I diabetes in a Caucasian population
K Sangthongpitag, K R Moore, N M Lapsys, et al.
American Journal of Human Genetics
|
November 1, 1989
Refined physical and genetic mapping of the NF1 region on chromosome 17
P R Fain, D E Goldgar, M R Wallace, et al.
American Journal of Human Genetics
|
March 21, 2000
X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3
C L Bennett, R Yoshioka, H Kiyosawa, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 53) with videos related to
Sort By:
Page
of 6
Diabetes
|
December 4, 1998
Transmission of DQ haplotypes to patients with type 1 diabetes
E Kawasaki, J Noble, H Erlich, et al.
JAMA
|
September 11, 1981
Survival in hereditary breast and colon cancer
H T Lynch, W A Albano, J A Recabaren, et al.
Neurology
|
April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia
F Cambi, X M Tang, P Cordray, et al.
Cancer
|
June 1, 1981
Familial breast cancer and its recognition in an oncology clinic
H T Lynch, P R Fain, D Golgar, et al.
The New England Journal of Medicine
|
October 6, 1988
Linkage heterogeneity of autosomal dominant polycystic kidney disease
W J Kimberling, P R Fain, J B Kenyon, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1982
Genetic/epidemiological findings in a study of smoking-associated tumors
H T Lynch, P R Fain, W A Albano, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets gene
M J Econs, D F Barker, M C Speer, et al.
Human Heredity
|
November 14, 1998
No evidence for linkage of a novel CA repeat polymorphism for apoptosis antigen 1 (APO-1 or fas) with type I diabetes in a Caucasian population
K Sangthongpitag, K R Moore, N M Lapsys, et al.
American Journal of Human Genetics
|
November 1, 1989
Refined physical and genetic mapping of the NF1 region on chromosome 17
P R Fain, D E Goldgar, M R Wallace, et al.
American Journal of Human Genetics
|
March 21, 2000
X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3
C L Bennett, R Yoshioka, H Kiyosawa, et al.
Page
of 6