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 492
... risk is 0.06 for any sibling of an IDDM proband ; 2 ) the probability is 0.25 to a sibling to carry also HLA - DR3 / 4 ; 3 ) X is the risk to a sibling who carries DR3 / 4 ( X 3.3Y ) ; and 4 ) Y is the risk to a sibling who does not ...
... risk is 0.06 for any sibling of an IDDM proband ; 2 ) the probability is 0.25 to a sibling to carry also HLA - DR3 / 4 ; 3 ) X is the risk to a sibling who carries DR3 / 4 ( X 3.3Y ) ; and 4 ) Y is the risk to a sibling who does not ...
Seite 493
... risk figures , not of the recurrence of a particular disease , but the overall risk for a disorder in the offspring of consanguineous matings . The risk can be estimated in two ways either theoretically or empirically . The theoretical ...
... risk figures , not of the recurrence of a particular disease , but the overall risk for a disorder in the offspring of consanguineous matings . The risk can be estimated in two ways either theoretically or empirically . The theoretical ...
Seite 517
... risk and in assessing one's ability to cope with the worst . From the outset , the parents appear to be engaged in a process of risk assessment , trying to make sense of and determine the manageability of the risk they face should they ...
... risk and in assessing one's ability to cope with the worst . From the outset , the parents appear to be engaged in a process of risk assessment , trying to make sense of and determine the manageability of the risk they face should they ...
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