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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... parents of children in the mut and cbl B classes . We found about half of normal mutase activity in two parents of muro mutants and five parents of mur mutants , demonstrating that obligate heterozygotes for these disorders can be ...
... parents of children in the mut and cbl B classes . We found about half of normal mutase activity in two parents of muro mutants and five parents of mur mutants , demonstrating that obligate heterozygotes for these disorders can be ...
Seite 244
... Parents ( Matsunaga , 1981 ) Affected children Bilateral Unilateral Mean age Mean age Expressivity of carrier parents Bilaterality ( % ) No. ( mo ) No. ( mo ) Unaffected Unilateral 9 2 24.6 7.0 35 4 31.9 25.5 20.5 33.3 that , if there ...
... Parents ( Matsunaga , 1981 ) Affected children Bilateral Unilateral Mean age Mean age Expressivity of carrier parents Bilaterality ( % ) No. ( mo ) No. ( mo ) Unaffected Unilateral 9 2 24.6 7.0 35 4 31.9 25.5 20.5 33.3 that , if there ...
Seite 514
... parental role . Having had an abnormal child makes most women question their ability to be parents . ( This is particularly true of women whose firstborns are affected and who thereby lack evidence that they can have normal children ...
... parental role . Having had an abnormal child makes most women question their ability to be parents . ( This is particularly true of women whose firstborns are affected and who thereby lack evidence that they can have normal children ...
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