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 90
... common disease phenotypes . Thus , phenocopies by environmental agents can mimic diseases with a large genetic component , and different mutations ( genocopies ) can lead to similar phenotypes . Heterogeneity may not be detected because ...
... common disease phenotypes . Thus , phenocopies by environmental agents can mimic diseases with a large genetic component , and different mutations ( genocopies ) can lead to similar phenotypes . Heterogeneity may not be detected because ...
Seite 93
... common cancers seems clear . The most common cancer of 40 years ago , cancer of the stomach , is declining in frequency sharply , possibly because of better refrigeration in recent years with consequent removal of ingested natural ...
... common cancers seems clear . The most common cancer of 40 years ago , cancer of the stomach , is declining in frequency sharply , possibly because of better refrigeration in recent years with consequent removal of ingested natural ...
Seite 97
... Common Disease David L. Rimoin and Jerome I. Rotter Many common disorders with familial aggregation have been postulated to be inherited as polygenic traits , since the segregation ratios found do not fit any simple mode of inheritance ...
... Common Disease David L. Rimoin and Jerome I. Rotter Many common disorders with familial aggregation have been postulated to be inherited as polygenic traits , since the segregation ratios found do not fit any simple mode of inheritance ...
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