Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 208
... alleles at the ABO locus as determining the synthesis of alternative enzymes with qualitatively different specificities . The O allele on the other hand appears to be inactive , and presumably results in what can be considered in this ...
... alleles at the ABO locus as determining the synthesis of alternative enzymes with qualitatively different specificities . The O allele on the other hand appears to be inactive , and presumably results in what can be considered in this ...
Seite 210
... alleles occur with similar frequencies in the English and the Negro populations [ Spencer , Hopkinson , & Harris , 1964a ] . PGM , exhibits much less variation , but there is one allele found in about 1-2 per cent of the Negroes we have ...
... alleles occur with similar frequencies in the English and the Negro populations [ Spencer , Hopkinson , & Harris , 1964a ] . PGM , exhibits much less variation , but there is one allele found in about 1-2 per cent of the Negroes we have ...
Seite 250
... alleles within a system , Yasuda [ 1966 ] investigated a more general model under which each allele may have a characteristic inbreeding coefficient and so the frequency of the homozygote A¡A1 is på ( 1 − F ; ) + piFi , where A ; may ...
... alleles within a system , Yasuda [ 1966 ] investigated a more general model under which each allele may have a characteristic inbreeding coefficient and so the frequency of the homozygote A¡A1 is på ( 1 − F ; ) + piFi , where A ; may ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
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abnormal acatalasia acatalatic acid Acta activity alleles Amer amino-acid amino-acid sequence analysis aneuploidy anomalies antibodies antigenic autosomal dominant autosomal recessive biochemical birth blood blood-group catalase cent child chromosome aberrations clinical colonies congenital consanguinity Cytogenetics defect deficiency Dept determined disaccharidases disease distribution duplication effects enzyme evolution factors female gamma globulin gene frequencies hemoglobin heredity is autosomal heterochromatin heterozygotes heterozygous Hospital Human Genetics inactivation individuals inheritance intestinal karyotype L-leut lactase Lancet leukemia linkage loci locus male malformations maltase marker marriage mating Medical mental metabolism Michigan Mongolism mosaic mutation normal observed pairs parents patients pattern pedigree peptide chains Ph¹ phenotype population possible Proc protein recombination records red cells selection sex chromatin sex-linked specific structure studies substance sucrase syndrome synthesis Table techniques tion tissue traits translocation trisomy University variable variation X-chromosome York