Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
Ergebnisse 1-3 von 33
Seite 236
... inherited causes of disease in populations . ' Inherited ' is here used in a broad sense , to include both biological and cultural inheritance . The set of relatives may be as close as twins or as extended as an ethnic group . Genetic ...
... inherited causes of disease in populations . ' Inherited ' is here used in a broad sense , to include both biological and cultural inheritance . The set of relatives may be as close as twins or as extended as an ethnic group . Genetic ...
Seite 242
... inheritance , without major loci . Segregation analysis leads directly to specific recurrence risks , shown in much condensed form in Table 4. As can be seen , there is at least a 7 - fold variation in risk among families . One wonders ...
... inheritance , without major loci . Segregation analysis leads directly to specific recurrence risks , shown in much condensed form in Table 4. As can be seen , there is at least a 7 - fold variation in risk among families . One wonders ...
Seite 390
... inheritance of lactose malabsorption . For the 2 other family types the theoretical expectation for children with lactose malabsorption , assuming autosomal recessive inheritance , is 0.25 for Type 1 and 0.5 for Type 2. Both hypotheses ...
... inheritance of lactose malabsorption . For the 2 other family types the theoretical expectation for children with lactose malabsorption , assuming autosomal recessive inheritance , is 0.25 for Type 1 and 0.5 for Type 2. Both hypotheses ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
30 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel