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 37
Seite 20
... genome rates - given the estimated 3 × 109 nucleotide pairs in the human haploid genome and an average cistron length of 103 nucleotides have been difficult to face for a generation of geneticists swayed by Muller's argument ( 1950 ) ...
... genome rates - given the estimated 3 × 109 nucleotide pairs in the human haploid genome and an average cistron length of 103 nucleotides have been difficult to face for a generation of geneticists swayed by Muller's argument ( 1950 ) ...
Seite 91
... genome consists of various kinds of repetitive DNA's . Some of these repeated DNA's are non - contiguous palindromic sequences of around 300-1200 nucleotide pairs long , which are interspersed with single copy sequences and are ...
... genome consists of various kinds of repetitive DNA's . Some of these repeated DNA's are non - contiguous palindromic sequences of around 300-1200 nucleotide pairs long , which are interspersed with single copy sequences and are ...
Seite 282
... genomes ( less than 0.001 of the haploid genome ) may be functionally integrated into the host chromosome set . These procedures naturally lend themselves to gene mapping in mammalian species . Already , considerable information has ...
... genomes ( less than 0.001 of the haploid genome ) may be functionally integrated into the host chromosome set . These procedures naturally lend themselves to gene mapping in mammalian species . Already , considerable information has ...
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