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 286
... examples of the phenomenon of extinction in hybrid cells . The first example shown , that of hybrids between Syrian hamster pigmented TABLE 2 Examples of extinction : melanoma and hepatoma hybrids Parental cells Cross ( ploidy : diploid ...
... examples of the phenomenon of extinction in hybrid cells . The first example shown , that of hybrids between Syrian hamster pigmented TABLE 2 Examples of extinction : melanoma and hepatoma hybrids Parental cells Cross ( ploidy : diploid ...
Seite 347
... example is ataxia telangiectasia ( AT ) , which is associated with defects in excision repair that differ from those in XP ( Paterson et al . , 1976 ) . Other less well established examples include Bloom's syndrome , Cockayne's syndrome ...
... example is ataxia telangiectasia ( AT ) , which is associated with defects in excision repair that differ from those in XP ( Paterson et al . , 1976 ) . Other less well established examples include Bloom's syndrome , Cockayne's syndrome ...
Seite 406
... examples will occur and that some of these will result from analysis of such families as that reported by Smith and ... example , hepatoma occurs at high frequency among subjects with alpha , -antitrypsin deficiency , in which condition ...
... examples will occur and that some of these will result from analysis of such families as that reported by Smith and ... example , hepatoma occurs at high frequency among subjects with alpha , -antitrypsin deficiency , in which condition ...
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