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 361
... patient with the same association of aniridia and nephroblastoma . At the same time , Andersen et al ( 1978 ) reported a del ( 11p ) in a patient with aniridia and gonadoblastoma but without Wilms tumor . Some 12 patients with the ...
... patient with the same association of aniridia and nephroblastoma . At the same time , Andersen et al ( 1978 ) reported a del ( 11p ) in a patient with aniridia and gonadoblastoma but without Wilms tumor . Some 12 patients with the ...
Seite 468
... patients with high values are referred for ultrasonography and amniocentesis ( Wald et al , 1979 ) ; 2 ) after serum AFP determination , patients with elevated values are routinely retested before decisions are made about ...
... patients with high values are referred for ultrasonography and amniocentesis ( Wald et al , 1979 ) ; 2 ) after serum AFP determination , patients with elevated values are routinely retested before decisions are made about ...
Seite 580
... patients with Gaucher ( Brady et al , 1980 ; Beutler et al , 1980 ) and Fabry disease ( Desnick et al , 1980 ) , no immunologic reaction to glucocerebrosidase and a - galactosidase , respectively , was detectable after repeated enzyme ...
... patients with Gaucher ( Brady et al , 1980 ; Beutler et al , 1980 ) and Fabry disease ( Desnick et al , 1980 ) , no immunologic reaction to glucocerebrosidase and a - galactosidase , respectively , was detectable after repeated enzyme ...
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