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 86
... evidence for the presence of one DNA duplex per chromatid . 5. Finally , the fifth piece of evidence is quite different and relates to the composition of DNA present in the genome . If each chromatid contained a bundle of identical DNA ...
... evidence for the presence of one DNA duplex per chromatid . 5. Finally , the fifth piece of evidence is quite different and relates to the composition of DNA present in the genome . If each chromatid contained a bundle of identical DNA ...
Seite 360
... evidence of sensitivity to X - rays ( Cunliffe et al . , 1974 ) , experi- mental evidence of a DNA repair defect ( Paterson et al . , 1976 ) and of sensitivity to X - rays ( Taylor et al . , 1975 , 1976 ) , in vivo evidence of clone ...
... evidence of sensitivity to X - rays ( Cunliffe et al . , 1974 ) , experi- mental evidence of a DNA repair defect ( Paterson et al . , 1976 ) and of sensitivity to X - rays ( Taylor et al . , 1975 , 1976 ) , in vivo evidence of clone ...
Seite 362
... evidence for a specific 8/21 translocation ( Rowley , 1975 ; Oshimura et al . , 1976a ) . In meningiomas there appears to be a specific loss of chromosome 22 and even in the few cases that are hyper diploid there is a relative ...
... evidence for a specific 8/21 translocation ( Rowley , 1975 ; Oshimura et al . , 1976a ) . In meningiomas there appears to be a specific loss of chromosome 22 and even in the few cases that are hyper diploid there is a relative ...
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