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 97
... disorders with familial aggregation have been postulated to be inherited as polygenic traits , since the segregation ratios found do not fit any simple mode of inheritance . In recent years , however , it has become apparent that for ...
... disorders with familial aggregation have been postulated to be inherited as polygenic traits , since the segregation ratios found do not fit any simple mode of inheritance . In recent years , however , it has become apparent that for ...
Seite 98
... disorder ? These disorders are sufficiently common that the different forms may occasionally occur in the same family by chance alone . Both are chronic diseases that may manifest in early life but increase in frequency with age . Both ...
... disorder ? These disorders are sufficiently common that the different forms may occasionally occur in the same family by chance alone . Both are chronic diseases that may manifest in early life but increase in frequency with age . Both ...
Seite 211
... disorders at several levels — those of gene structure and function , of protein structure , of altered cell physiology , or of tissue pathophysiology . For some disorders the understanding is detailed and the relationship among altered ...
... disorders at several levels — those of gene structure and function , of protein structure , of altered cell physiology , or of tissue pathophysiology . For some disorders the understanding is detailed and the relationship among altered ...
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