Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 157
... activity , the latter 25 per cent of the maltase and sucrase activity . From an analysis of the kinetics of heat inactivation , Dahlqvist concluded that maltase Ia , Ib , II , and III are four different " single " enzymes [ 22 ] . At ...
... activity , the latter 25 per cent of the maltase and sucrase activity . From an analysis of the kinetics of heat inactivation , Dahlqvist concluded that maltase Ia , Ib , II , and III are four different " single " enzymes [ 22 ] . At ...
Seite 161
... activity appears at gestation time . Its development in the embryo is not prevented by mastectomy [ 27 ] . The activity reaches a maximum at birth or shortly after birth . In premature infants , the level of B - galactosidase is low at ...
... activity appears at gestation time . Its development in the embryo is not prevented by mastectomy [ 27 ] . The activity reaches a maximum at birth or shortly after birth . In premature infants , the level of B - galactosidase is low at ...
Seite 194
... activity . This is also true for acatalasia . Already in his early papers Takahara [ 5 ] stated that acatalatic blood exerts 1 / 450-1 / 900 of normal activity . However , there is a considerable scattering where the level of residual ...
... activity . This is also true for acatalasia . Already in his early papers Takahara [ 5 ] stated that acatalatic blood exerts 1 / 450-1 / 900 of normal activity . However , there is a considerable scattering where the level of residual ...
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