Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 65
... Enzyme activity is altered , but is a less precise determinant of genotype [ 16 , 17 ] . B. ( 2 ) Demonstration of deficiency of activity of an enzyme . In some conditions this may be the result of a change in the structure of a protein ...
... Enzyme activity is altered , but is a less precise determinant of genotype [ 16 , 17 ] . B. ( 2 ) Demonstration of deficiency of activity of an enzyme . In some conditions this may be the result of a change in the structure of a protein ...
Seite 203
... enzyme ( s ) . Lack of an enzyme is not necessarily due to repression or any other alteration within the controller gene system ; it may just as well be due to the synthesis of a variant enzyme of reduced stability — as seems to be the ...
... enzyme ( s ) . Lack of an enzyme is not necessarily due to repression or any other alteration within the controller gene system ; it may just as well be due to the synthesis of a variant enzyme of reduced stability — as seems to be the ...
Seite 209
... enzyme is determined by at least one gene locus and that there are probably other loci which control the rates of synthesis of specific enzymes or groups of enzymes . In effect then one is asking at what proportion of this large array ...
... enzyme is determined by at least one gene locus and that there are probably other loci which control the rates of synthesis of specific enzymes or groups of enzymes . In effect then one is asking at what proportion of this large array ...
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