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Nature Genetics
|
July 1, 1993
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
T R Prezant, J V Agapian, M C Bohlman, et al.
Human Heredity
|
January 1, 1984
Estimating the recombination frequency for the MN and the Ss loci
M A Spence, L L Field, M L Marazita, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2001
Autoantibodies and human leucocyte antigen class II in first-degree family members of Mexican-American type 1 diabetic patients
A Zeidler, L J Raffel, G Costin, et al.
Scandinavian Journal of Gastroenterology. Supplement
|
January 1, 1983
Pathological acid secretion not due to gastrinoma
J H Walsh, P K Nair, J Kleibeuker, et al.
American Journal of Human Genetics
|
July 31, 1998
Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype
H Allayee, B E Aouizerat, R M Cantor, et al.
Diabetes
|
July 1, 1992
Genetic marker associations with proliferative retinopathy in persons diagnosed with diabetes before 30 yr of age
K J Cruickshanks, C M Vadheim, S E Moss, et al.
American Journal of Human Genetics
|
June 1, 1986
Relationships between the human pepsinogen DNA and protein polymorphisms
R T Taggart, I M Samloff, L J Raffel, et al.
Molecular Genetics and Metabolism
|
December 16, 1998
Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus
M Shohat, R Lotan, N Magal, et al.
Human Reproduction (Oxford, England)
|
November 30, 2018
Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndrome
M A Brower, Y Hai, M R Jones, et al.
Lancet (London, England)
|
October 24, 1981
Close genetic linkage between diabetes mellitus and kidd blood group
S E Hodge, C E Anderson, K Neiswanger, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 214) with videos related to
Sort By:
Page
of 22
Nature Genetics
|
July 1, 1993
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
T R Prezant, J V Agapian, M C Bohlman, et al.
Human Heredity
|
January 1, 1984
Estimating the recombination frequency for the MN and the Ss loci
M A Spence, L L Field, M L Marazita, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2001
Autoantibodies and human leucocyte antigen class II in first-degree family members of Mexican-American type 1 diabetic patients
A Zeidler, L J Raffel, G Costin, et al.
Scandinavian Journal of Gastroenterology. Supplement
|
January 1, 1983
Pathological acid secretion not due to gastrinoma
J H Walsh, P K Nair, J Kleibeuker, et al.
American Journal of Human Genetics
|
July 31, 1998
Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype
H Allayee, B E Aouizerat, R M Cantor, et al.
Diabetes
|
July 1, 1992
Genetic marker associations with proliferative retinopathy in persons diagnosed with diabetes before 30 yr of age
K J Cruickshanks, C M Vadheim, S E Moss, et al.
American Journal of Human Genetics
|
June 1, 1986
Relationships between the human pepsinogen DNA and protein polymorphisms
R T Taggart, I M Samloff, L J Raffel, et al.
Molecular Genetics and Metabolism
|
December 16, 1998
Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus
M Shohat, R Lotan, N Magal, et al.
Human Reproduction (Oxford, England)
|
November 30, 2018
Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndrome
M A Brower, Y Hai, M R Jones, et al.
Lancet (London, England)
|
October 24, 1981
Close genetic linkage between diabetes mellitus and kidd blood group
S E Hodge, C E Anderson, K Neiswanger, et al.
Page
of 22