Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 133
... possible to explain her abnormal development on the basis of a major autosomal duplication translocated to a terminal position on the long arm of an X. Further , it was possible to learn that the influ- ence of the X - heterochromatin ...
... possible to explain her abnormal development on the basis of a major autosomal duplication translocated to a terminal position on the long arm of an X. Further , it was possible to learn that the influ- ence of the X - heterochromatin ...
Seite 223
... possible to distinguish between 1 and 2 , even after determining the amino - acid sequence of the protein , depending upon the extent to which secondary , tertiary , and quaternary structure affect the antigenic site . If the antigen is ...
... possible to distinguish between 1 and 2 , even after determining the amino - acid sequence of the protein , depending upon the extent to which secondary , tertiary , and quaternary structure affect the antigenic site . If the antigen is ...
Seite 310
... possible are in sight . But in practice we are so far from it that few people recognize that it is attainable at all . Medical records in this country [ i.e. , in Britain ] are seldom short of chaos ; this is true often enough for the ...
... possible are in sight . But in practice we are so far from it that few people recognize that it is attainable at all . Medical records in this country [ i.e. , in Britain ] are seldom short of chaos ; this is true often enough for the ...
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