Human Genetics. Proceedings of the 6th International Congress..., Sept. 13-18, 1981, Jerusalem: Medical aspects. II, Teil 2Batsheva Bonné-Tamir Liss, 1982 - 619 Seiten |
Im Buch
Ergebnisse 1-3 von 63
Seite 49
... finding of a low DR3 frequency in lepromatous leprosy versus a high in tuberculoid leprosy has not been observed in other ... findings one could ( once more ) speculate that for the survival of the species it might be useful to have ...
... finding of a low DR3 frequency in lepromatous leprosy versus a high in tuberculoid leprosy has not been observed in other ... findings one could ( once more ) speculate that for the survival of the species it might be useful to have ...
Seite 223
... finding of lower ( ~ 10 - fold less ) residual a - neuraminidase activity and more rapid substrate accumulation . In addition to the common findings of cherry red macula , progressive blindness , and myoclonus , type 2 patients have an ...
... finding of lower ( ~ 10 - fold less ) residual a - neuraminidase activity and more rapid substrate accumulation . In addition to the common findings of cherry red macula , progressive blindness , and myoclonus , type 2 patients have an ...
Seite 352
... findings , IP may prove to be divisible into at least two groups . However , any subdivision of IP is premature at ... finding in essentially all FA patients ( Schroeder et al , 1964 ; Bloom et al , 1966 ) . Breaks are chromatid in type ...
... findings , IP may prove to be divisible into at least two groups . However , any subdivision of IP is premature at ... finding in essentially all FA patients ( Schroeder et al , 1964 ; Bloom et al , 1966 ) . Breaks are chromatid in type ...
Inhalt
Carrier Detection | 15 |
HLA and Infectious Diseases | 37 |
HLA and Diabetes | 55 |
Urheberrecht | |
49 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
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