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 150
... screening are discussed as part of the course material ( Clow and Scriver , 1977 ) . In answer to a specific question about the importance of genetic screening we found that 83.0 % of informed high school students agree that genetic ...
... screening are discussed as part of the course material ( Clow and Scriver , 1977 ) . In answer to a specific question about the importance of genetic screening we found that 83.0 % of informed high school students agree that genetic ...
Seite 170
... screening because they were based on retrospective estimates of the birth incidence of Down's syndrome in older mothers , which antenatal screening indicates may be much greater . They showed that such screening would be economic for ...
... screening because they were based on retrospective estimates of the birth incidence of Down's syndrome in older mothers , which antenatal screening indicates may be much greater . They showed that such screening would be economic for ...
Seite 219
... screening and confirms what has been observed previously in developed countries ( National Research Council Committee for the Study of Inborn Errors of Metabolism , 1975 ) . In the hospital where screening was part of the normal ...
... screening and confirms what has been observed previously in developed countries ( National Research Council Committee for the Study of Inborn Errors of Metabolism , 1975 ) . In the hospital where screening was part of the normal ...
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