Human Genetics. Proceedings of the 6th International Congress..., Sept. 13-18, 1981, Jerusalem: Medical aspects. II, Teil 2Batsheva Bonné-Tamir Liss, 1982 - 619 Seiten |
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Seite 67
... significant in female siblings ( P < 6.0 x 104 ) , but not significant in male siblings , partly because of the small number of male patients in these families . The strong association between the development of Graves disease and HLA ...
... significant in female siblings ( P < 6.0 x 104 ) , but not significant in male siblings , partly because of the small number of male patients in these families . The strong association between the development of Graves disease and HLA ...
Seite 77
... significant associations to the development of models to aid in the determination of the mode of inheritance of the disease . The initial HLA disease studies involved disease and control population data in a search to detect the ...
... significant associations to the development of models to aid in the determination of the mode of inheritance of the disease . The initial HLA disease studies involved disease and control population data in a search to detect the ...
Seite 115
... significant correlation between coronary score from coronary angiography and Lp ( a ) lipoprotein . Norwegian CHD patients had an Lp ( a + ) frequency of 66 % whereas the frequency in healthy people was 35 % . The relative risk in Lp ...
... significant correlation between coronary score from coronary angiography and Lp ( a ) lipoprotein . Norwegian CHD patients had an Lp ( a + ) frequency of 66 % whereas the frequency in healthy people was 35 % . The relative risk in Lp ...
Inhalt
Carrier Detection | 15 |
HLA and Infectious Diseases | 37 |
HLA and Diabetes | 55 |
Urheberrecht | |
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abnormalities activity addition affected allele analysis antigens appears association binding biochemical blood carrier cells changes chromosome clinical common complex cultured defect deficiency Department determined diabetes diabetes mellitus diagnosis disease disorders distribution dominant environmental enzyme estimated et al evidence expression factors fibroblasts findings frequency gene glucose haplotypes heterogeneity heterozygotes Hum Genet human hypertension IDDM immune important increased indicated individuals inheritance internalization involved Italy levels linkage linked locus lysosomal major marker measured Medical method mode of inheritance multiple mutant neural tube normal observed occur origin pairs parents patients phenotype population possible pregnancy prenatal present problems protein recently receptor recessive relative reported Research response risk screening showed shown significant specific structure studies suggested syndrome Table tissue trait translocation tumor twin ulcer University values York