Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 123
... structural rearrangements of chromosomes , has been found to be associated with congenital anomaly in hundreds of cases , and a few clinical syn- dromes caused by structural rearrangements which result in deficiency of chromo- somal ...
... structural rearrangements of chromosomes , has been found to be associated with congenital anomaly in hundreds of cases , and a few clinical syn- dromes caused by structural rearrangements which result in deficiency of chromo- somal ...
Seite 317
... structural genes and to reconstruct the evolution of these genes . Amino - acid sequences are direct translations of structural genes and may reveal the past evolutionary history of these genes . The amino - acid sequences of proteins ...
... structural genes and to reconstruct the evolution of these genes . Amino - acid sequences are direct translations of structural genes and may reveal the past evolutionary history of these genes . The amino - acid sequences of proteins ...
Seite 330
... structural gene only is responsible for the synthesis of the entire light chain , since it seems unlikely that multiple genes can diverge in exactly the same way . If there is only one structural gene for the synthesis of each type of ...
... structural gene only is responsible for the synthesis of the entire light chain , since it seems unlikely that multiple genes can diverge in exactly the same way . If there is only one structural gene for the synthesis of each type of ...
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