Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 155
... groups of conditions can be divided , for purposes of general biological , prognostic , pathogenetic and other considerations , into 4 major groups ( Herrmann and Opitz , 1974 ; Herrmann et al . , 1976 ; Opitz and Herrmann , 1976a , b ) ...
... groups of conditions can be divided , for purposes of general biological , prognostic , pathogenetic and other considerations , into 4 major groups ( Herrmann and Opitz , 1974 ; Herrmann et al . , 1976 ; Opitz and Herrmann , 1976a , b ) ...
Seite 259
... groups and the average genetic distance between them . Using allelic frequency data from the literature , this relationship was used to predict 87 % correct allocation for a set of racial groups , including Amerindians , Eskimoes ...
... groups and the average genetic distance between them . Using allelic frequency data from the literature , this relationship was used to predict 87 % correct allocation for a set of racial groups , including Amerindians , Eskimoes ...
Seite 349
... group will be found to apply universally . All 6 groups of XP are found in Europe and America , Group C being most common , Group A less common , Groups D , E and variant less still . Group B contains only a single representative ...
... group will be found to apply universally . All 6 groups of XP are found in Europe and America , Group C being most common , Group A less common , Groups D , E and variant less still . Group B contains only a single representative ...
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