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 15
... studies Much of the effort of human population genetics has been devoted to detecting and estimating genetic variance for human variable phenotypes . Such studies include normal variation such as for so - called ' cognitive ability ' or ...
... studies Much of the effort of human population genetics has been devoted to detecting and estimating genetic variance for human variable phenotypes . Such studies include normal variation such as for so - called ' cognitive ability ' or ...
Seite 17
... studies of some primitive ' cultures , like the monumental work on the Orinocan - Amazonian Indians . Both kinds of studies have made an immense contribution to our knowledge of the genetic variations in our species both within and ...
... studies of some primitive ' cultures , like the monumental work on the Orinocan - Amazonian Indians . Both kinds of studies have made an immense contribution to our knowledge of the genetic variations in our species both within and ...
Seite 182
... studies involving over 2000 amniocenteses have been published . One of those studies was carried out in the U.S.A. ( NICHD , 1976 ) and one in Canada ( Simpson et al . , 1976 ) . The results indicated that , under the conditions of each ...
... studies involving over 2000 amniocenteses have been published . One of those studies was carried out in the U.S.A. ( NICHD , 1976 ) and one in Canada ( Simpson et al . , 1976 ) . The results indicated that , under the conditions of each ...
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