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JAMA
|
December 11, 1999
The heritability of otitis media: a twin and triplet study
M L Casselbrant, E M Mandel, P A Fall, et al.
American Journal of Ophthalmology
|
September 1, 1982
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome
H M Hittner, R A King, V M Riccardi, et al.
The American Journal of Cardiology
|
January 15, 1993
Relation of apolipoprotein E phenotype to myocardial infarction and mortality from coronary artery disease
J E Eichner, L H Kuller, T J Orchard, et al.
Genetic Epidemiology
|
January 1, 1997
Gender-specific nonrandom association between the alpha 1-antichymotrypsin and apolipoprotein E polymorphisms in the general population and its implication for the risk of Alzheimer's disease
M I Kamboh, D K Sanghera, C E Aston, et al.
Human Molecular Genetics
|
November 18, 1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneity
R E Ferrell, K L Levinson, J H Esman, et al.
Journal of the American Geriatrics Society
|
March 14, 2002
Moderate physical activity is associated with higher bone mineral density in postmenopausal women
J M Hagberg, J M Zmuda, S D McCole, et al.
The Journal of Pediatrics
|
August 4, 1999
Correlates of lipoprotein(a) levels in a biracial cohort of young girls: the NHLBI Growth and Health Study
S Y Kimm, A Pasagian-Macaulay, C E Aston, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas
A Chakravarti, P P Majumder, S A Slaugenhaupt, et al.
Human Heredity
|
January 1, 1991
Genetic polymorphisms in southwest Alaskan Eskimos
G M Petersen, J I Ward, P I Terasaki, et al.
Mutation Research
|
January 27, 1999
Trinucleotide repeat length variation in the human ribosomal protein L14 gene (RPL14): localization to 3p21.3 and loss of heterozygosity in lung and oral cancers
S P Shriver, M D Shriver, D L Tirpak, et al.
Page
of 38
Search research articles
Search
Showing results (301-310 of 371) with videos related to
Sort By:
Page
of 38
JAMA
|
December 11, 1999
The heritability of otitis media: a twin and triplet study
M L Casselbrant, E M Mandel, P A Fall, et al.
American Journal of Ophthalmology
|
September 1, 1982
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome
H M Hittner, R A King, V M Riccardi, et al.
The American Journal of Cardiology
|
January 15, 1993
Relation of apolipoprotein E phenotype to myocardial infarction and mortality from coronary artery disease
J E Eichner, L H Kuller, T J Orchard, et al.
Genetic Epidemiology
|
January 1, 1997
Gender-specific nonrandom association between the alpha 1-antichymotrypsin and apolipoprotein E polymorphisms in the general population and its implication for the risk of Alzheimer's disease
M I Kamboh, D K Sanghera, C E Aston, et al.
Human Molecular Genetics
|
November 18, 1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneity
R E Ferrell, K L Levinson, J H Esman, et al.
Journal of the American Geriatrics Society
|
March 14, 2002
Moderate physical activity is associated with higher bone mineral density in postmenopausal women
J M Hagberg, J M Zmuda, S D McCole, et al.
The Journal of Pediatrics
|
August 4, 1999
Correlates of lipoprotein(a) levels in a biracial cohort of young girls: the NHLBI Growth and Health Study
S Y Kimm, A Pasagian-Macaulay, C E Aston, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas
A Chakravarti, P P Majumder, S A Slaugenhaupt, et al.
Human Heredity
|
January 1, 1991
Genetic polymorphisms in southwest Alaskan Eskimos
G M Petersen, J I Ward, P I Terasaki, et al.
Mutation Research
|
January 27, 1999
Trinucleotide repeat length variation in the human ribosomal protein L14 gene (RPL14): localization to 3p21.3 and loss of heterozygosity in lung and oral cancers
S P Shriver, M D Shriver, D L Tirpak, et al.
Page
of 38