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 80
... Dominant 3.5 69.5 Hemochromatosis ( Simon et al , 1977a ; Kidd , 1979 ] A3 / A3 A3 / — 6 21.3 6.0 Total 79 individuals xi = 47.55 , P < 0.001 xi = 0.097 , NS Observed 20 43 Recessive 20.5 42.0 Dominant 8.8 55.0 Multiple sclerosis ...
... Dominant 3.5 69.5 Hemochromatosis ( Simon et al , 1977a ; Kidd , 1979 ] A3 / A3 A3 / — 6 21.3 6.0 Total 79 individuals xi = 47.55 , P < 0.001 xi = 0.097 , NS Observed 20 43 Recessive 20.5 42.0 Dominant 8.8 55.0 Multiple sclerosis ...
Seite 81
... dominant mode of inheritance can also be ruled out for the HLA - linked IDDM gene in this case ( Thomson , manuscript in preparation ) . Greenberg et al ( 1982 ] have analyzed DR3 and DR7 genotypic data for celiac disease . Their ...
... dominant mode of inheritance can also be ruled out for the HLA - linked IDDM gene in this case ( Thomson , manuscript in preparation ) . Greenberg et al ( 1982 ] have analyzed DR3 and DR7 genotypic data for celiac disease . Their ...
Seite 82
... dominant and recessive modes of inheritance are compatible with the data . For a dominant mode of inheritance the estimated value of pp is 0.21 ( SD 0.08 ) ; for a recessive mode of inheritance the estimated value of po is much higher ...
... dominant and recessive modes of inheritance are compatible with the data . For a dominant mode of inheritance the estimated value of pp is 0.21 ( SD 0.08 ) ; for a recessive mode of inheritance the estimated value of po is much higher ...
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