Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 141
... evolution thus established in human leukemias received further support from new observations . Clonal evolutions proceed either by acquisi- tion of extra chromosomes , by loss of chromosomes , or by a combination of both mechanisms ...
... evolution thus established in human leukemias received further support from new observations . Clonal evolutions proceed either by acquisi- tion of extra chromosomes , by loss of chromosomes , or by a combination of both mechanisms ...
Seite 320
... evolution of the hemoglobin genes in different species and to correlate gene duplications with steps in speciation . Presumably the evolution of the hemoglobin and myoglobin genes has followed a similar , but not identical , pattern in ...
... evolution of the hemoglobin genes in different species and to correlate gene duplications with steps in speciation . Presumably the evolution of the hemoglobin and myoglobin genes has followed a similar , but not identical , pattern in ...
Seite 328
... evolution ; this is a possible evolutionary pathway for the appear- ance in evolution of allosteric proteins . RATE OF EVOLUTION OF DIFFERENT PROTEINS The rate at which amino - acid replacements may appear and accumulate in pro- teins ...
... evolution ; this is a possible evolutionary pathway for the appear- ance in evolution of allosteric proteins . RATE OF EVOLUTION OF DIFFERENT PROTEINS The rate at which amino - acid replacements may appear and accumulate in pro- teins ...
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