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 89
... references ) . The role of genes rather than a common familial environment alone has been suggested by twin and adoption studies in many instances . The resemblance of biologic sibs in different environments and the absence of spouse ...
... references ) . The role of genes rather than a common familial environment alone has been suggested by twin and adoption studies in many instances . The resemblance of biologic sibs in different environments and the absence of spouse ...
Seite 92
... references ) . There may be interaction of specified genetic systems . Thus , slow acetylation status plus the possession of a certain HLA D type makes for a higher frequency of lupus erythematosus following administration of ...
... references ) . There may be interaction of specified genetic systems . Thus , slow acetylation status plus the possession of a certain HLA D type makes for a higher frequency of lupus erythematosus following administration of ...
Seite 142
... reference to the X chromosome , where errors are easily made in relation to even simple relationships . The possible use of correlated biochemical variation as an aid to the diagnosis of the main defect was discussed by Professor ...
... reference to the X chromosome , where errors are easily made in relation to even simple relationships . The possible use of correlated biochemical variation as an aid to the diagnosis of the main defect was discussed by Professor ...
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