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 280
... mouse microcell hybrid . The preparation has been stained by the alkaline Giemsa procedure ( Friend et al . , 1976 ) , which stains human and mouse chromosomes differentially . The arrow indicates human chromosome 17 . A second way to ...
... mouse microcell hybrid . The preparation has been stained by the alkaline Giemsa procedure ( Friend et al . , 1976 ) , which stains human and mouse chromosomes differentially . The arrow indicates human chromosome 17 . A second way to ...
Seite 281
... Mouse Cells Express Human HPRT } HAT Selection 1000 RECIPIENT Mouse Cells HPRT- Fig . 4. Chromosome - mediated gene transfer scheme . See text . found in mouse ( HPRT- ) → mouse ( HPRT + ) transgenotes that donor HPRT ( in this case a ...
... Mouse Cells Express Human HPRT } HAT Selection 1000 RECIPIENT Mouse Cells HPRT- Fig . 4. Chromosome - mediated gene transfer scheme . See text . found in mouse ( HPRT- ) → mouse ( HPRT + ) transgenotes that donor HPRT ( in this case a ...
Seite 287
... mouse melanoma cells and mouse L cell fibroblasts were also unpigmented . The second , third and fourth examples shown in Table 2 concern crosses performed with well differentiated rat hepatoma cells and cells of the same or different ...
... mouse melanoma cells and mouse L cell fibroblasts were also unpigmented . The second , third and fourth examples shown in Table 2 concern crosses performed with well differentiated rat hepatoma cells and cells of the same or different ...
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