Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 321
... amino - acid sequences . Since a chains are associated with all the other hemo- globin peptide chains to form functional hemoglobin molecules , it seemed logical that changes in the a chains which affect all the hemoglobins of one ...
... amino - acid sequences . Since a chains are associated with all the other hemo- globin peptide chains to form functional hemoglobin molecules , it seemed logical that changes in the a chains which affect all the hemoglobins of one ...
Seite 322
... Amino - acid sequence of the a peptide chain of hemoglobin of different species . The amino - acid residues are indicated by a one- letter code [ Dayhoff et al . , 1965 ] . The amino - acid sequence of the human a chain only is entirely ...
... Amino - acid sequence of the a peptide chain of hemoglobin of different species . The amino - acid residues are indicated by a one- letter code [ Dayhoff et al . , 1965 ] . The amino - acid sequence of the human a chain only is entirely ...
Seite 330
... amino - acid interchanges have been shown in the NH2 - terminal half . One amino - acid interchange only has been shown to occur in the COOH - terminal half of the K - type human light chains . This amino - acid interchange , a leucine ...
... amino - acid interchanges have been shown in the NH2 - terminal half . One amino - acid interchange only has been shown to occur in the COOH - terminal half of the K - type human light chains . This amino - acid interchange , a leucine ...
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