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 64
Seite 55
... methods are available in this field . I shall present results obtained by two of these methods . The fourth approach , SCE scoring , is a new and very promising one . It is not yet possible to give a definite assessment , but it looks ...
... methods are available in this field . I shall present results obtained by two of these methods . The fourth approach , SCE scoring , is a new and very promising one . It is not yet possible to give a definite assessment , but it looks ...
Seite 245
... methods of reducing the information in the genetic distance matrix to dimensions which can be visualized have been employed . The first is the construction of dendrograms , or networks using either ' divisive ' or ' agglomerative ...
... methods of reducing the information in the genetic distance matrix to dimensions which can be visualized have been employed . The first is the construction of dendrograms , or networks using either ' divisive ' or ' agglomerative ...
Seite 270
... methods interact synergistically , and together provide a powerful tool for mapping the human genome . Presently , a ... method of gene transfer in mammalian cell systems . This method was pioneered by Ege and Ringertz ( 1974 ) . The ...
... methods interact synergistically , and together provide a powerful tool for mapping the human genome . Presently , a ... method of gene transfer in mammalian cell systems . This method was pioneered by Ege and Ringertz ( 1974 ) . The ...
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