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 65
... increased numbers of chromosome breaks and exchanges ( either spontaneous or after treatment ) , and a tendency to form clones of cells with mutant karyotypes . The increased number of chromosomal gaps and breaks in these disorders has ...
... increased numbers of chromosome breaks and exchanges ( either spontaneous or after treatment ) , and a tendency to form clones of cells with mutant karyotypes . The increased number of chromosomal gaps and breaks in these disorders has ...
Seite 67
... increased chromosome instability ( i.e. with an increased chromosome mutation rate ) and cancer has been recognized . Each of the genes occurs at a low frequency in the population , and the diseases which occur in persons homozygous for ...
... increased chromosome instability ( i.e. with an increased chromosome mutation rate ) and cancer has been recognized . Each of the genes occurs at a low frequency in the population , and the diseases which occur in persons homozygous for ...
Seite 405
... increased mutation rate , presumably at all genetic loci , including those that lead to cancer . Two somatic mutations are evidently required at some such locus to produce cancer , but each occurs at a greatly increased rate . In the ...
... increased mutation rate , presumably at all genetic loci , including those that lead to cancer . Two somatic mutations are evidently required at some such locus to produce cancer , but each occurs at a greatly increased rate . In the ...
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