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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... mutant lines provided direct evidence that the inherited methylmalonic acidemias are recessively inherited ( Willard and Rosenberg , 1979a ; Gravel et al , 1975 ) . This conclusion derives from the finding that each mutation can be ...
... mutant lines provided direct evidence that the inherited methylmalonic acidemias are recessively inherited ( Willard and Rosenberg , 1979a ; Gravel et al , 1975 ) . This conclusion derives from the finding that each mutation can be ...
Seite 249
... mutation model : Carotid body tumors and retinoblastoma . In Mulvihill JJ , Miller RW , Fraumeni JF Jr ( eds ) : “ Genetics of Human Cancer . " New York : Raven Press , pp 417–438 . Hethcote HW , Knudson AG Jr ( 1978 ) : Model for the ...
... mutation model : Carotid body tumors and retinoblastoma . In Mulvihill JJ , Miller RW , Fraumeni JF Jr ( eds ) : “ Genetics of Human Cancer . " New York : Raven Press , pp 417–438 . Hethcote HW , Knudson AG Jr ( 1978 ) : Model for the ...
Seite 363
... mutation 90 % : Somatic , nonheritable mutation Chromosome aberration : 2-10 % retardation and del 11p13 . Hum Genet 57 : 300_306 The Aniridia and Retinoblastoma Stories / 363.
... mutation 90 % : Somatic , nonheritable mutation Chromosome aberration : 2-10 % retardation and del 11p13 . Hum Genet 57 : 300_306 The Aniridia and Retinoblastoma Stories / 363.
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