Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 57
... errors of metabolism are being discovered at a rapid rate . This is due to screening programs which were made possible by the development of simple chromatographic techniques and by bacterial inhibition assays . This report will ...
... errors of metabolism are being discovered at a rapid rate . This is due to screening programs which were made possible by the development of simple chromatographic techniques and by bacterial inhibition assays . This report will ...
Seite 208
... errors of metabolism . " For the same reason the Lea- allele at the Lewis locus can also be considered as analogous to the genes which determine the classical " inborn errors . " Thus the phenomena discovered by Landsteiner on the one ...
... errors of metabolism . " For the same reason the Lea- allele at the Lewis locus can also be considered as analogous to the genes which determine the classical " inborn errors . " Thus the phenomena discovered by Landsteiner on the one ...
Seite 278
... errors made in this study . Three individuals from a total of 732 ( 0.41 per cent ) had to be retested because they were originally typed MN in a family where all others were M. As a second check we examined the data for the fifty ...
... errors made in this study . Three individuals from a total of 732 ( 0.41 per cent ) had to be retested because they were originally typed MN in a family where all others were M. As a second check we examined the data for the fifty ...
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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Häufige Begriffe und Wortgruppen
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