Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
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Seite 66
... lines . Single - strand breaks rejoin normally ( Harnden , 1974 ; Paterson et al . , 1976a ; Taylor et al . , 1976 ) . Cell lines derived from individuals with this syndrome also appear to be abnormally sensitive to actinomycin D and ...
... lines . Single - strand breaks rejoin normally ( Harnden , 1974 ; Paterson et al . , 1976a ; Taylor et al . , 1976 ) . Cell lines derived from individuals with this syndrome also appear to be abnormally sensitive to actinomycin D and ...
Seite 263
... lines which are presently under study can be divided into two categories , ' pleokaryonic ' and ' isokaryonic ' . I have invented these words for this Congress , because all the terms I have previously used have been criticized . These ...
... lines which are presently under study can be divided into two categories , ' pleokaryonic ' and ' isokaryonic ' . I have invented these words for this Congress , because all the terms I have previously used have been criticized . These ...
Seite 265
... lines , whereas when the method has been selection of donors , the variant cells have been isokaryonic . One reason for this difference is that human isokaryonic lines can be isolated with high probability from any donor , whereas human ...
... lines , whereas when the method has been selection of donors , the variant cells have been isokaryonic . One reason for this difference is that human isokaryonic lines can be isolated with high probability from any donor , whereas human ...
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 | |
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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