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 113
... involved in genetic predisposition to CHD . Since the disease is frequent and the genetic component to its etiology significant , one would expect frequently occurring genes , such as those belonging to normal polymorphisms , to be involved ...
... involved in genetic predisposition to CHD . Since the disease is frequent and the genetic component to its etiology significant , one would expect frequently occurring genes , such as those belonging to normal polymorphisms , to be involved ...
Seite 238
... involved in a translocation with No. 8 carries a gene that would be of great importance in the normal function of a B - cell . What the role of 8q is in modifying this function so that the cell becomes a malignant B - cell is at present ...
... involved in a translocation with No. 8 carries a gene that would be of great importance in the normal function of a B - cell . What the role of 8q is in modifying this function so that the cell becomes a malignant B - cell is at present ...
Seite 450
... involved . This can be achieved through the communication of coded samples at regular intervals to all laboratories involved in such determinations . A central committee for quality control is then able to evaluate the results ...
... involved . This can be achieved through the communication of coded samples at regular intervals to all laboratories involved in such determinations . A central committee for quality control is then able to evaluate the results ...
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