Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 173
... substance has yet to be satisfactorily achieved in the test tube , sufficient of the assumptions inherent in the schemes have proved to be correct to make us feel that the actual steps in the synthesis cannot be far removed from those ...
... substance has yet to be satisfactorily achieved in the test tube , sufficient of the assumptions inherent in the schemes have proved to be correct to make us feel that the actual steps in the synthesis cannot be far removed from those ...
Seite 174
... substance is not converted to H substance , even when an H gene is present and therefore no A or B substances are formed . In the absence of the Le gene the precursor substance is converted in the presence of H and the Se genes to H ...
... substance is not converted to H substance , even when an H gene is present and therefore no A or B substances are formed . In the absence of the Le gene the precursor substance is converted in the presence of H and the Se genes to H ...
Seite 180
A - substance " A " enzyme ( -GalNAc ) H - substance " H " enzyme ( -Fucose ) B - substance " B " enzyme ( -Gal ) Lea - and Type XIV - active substance " Lea " enzyme Type XIV - active substance FIG . 6. Sequential enzymic degradation ...
A - substance " A " enzyme ( -GalNAc ) H - substance " H " enzyme ( -Fucose ) B - substance " B " enzyme ( -Gal ) Lea - and Type XIV - active substance " Lea " enzyme Type XIV - active substance FIG . 6. Sequential enzymic degradation ...
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