Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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... represent , or have attempted to represent , a tradition which has had a considerable effect in originating and moulding the science of human genetics . Those circumstances have arisen because Francis Galton , who initiated the ...
... represent , or have attempted to represent , a tradition which has had a considerable effect in originating and moulding the science of human genetics . Those circumstances have arisen because Francis Galton , who initiated the ...
Seite 221
... represent a distinct structural entity . The specificity P may differ from specificity Q by the substitution of a single amino acid or carbohydrate moiety , while the difference between X and Y may involve a similar substitution at some ...
... represent a distinct structural entity . The specificity P may differ from specificity Q by the substitution of a single amino acid or carbohydrate moiety , while the difference between X and Y may involve a similar substitution at some ...
Seite 229
... represent separate loci . However , we have only one value from the mouse with which to compare , and it is questionable whether we should try to extrapolate frequencies from Drosophila to mouse . Furthermore , in Drosophila , the ...
... represent separate loci . However , we have only one value from the mouse with which to compare , and it is questionable whether we should try to extrapolate frequencies from Drosophila to mouse . Furthermore , in Drosophila , 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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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