Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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... sequence has not been established . The amino - acid sequence of mouse [ Popp , 1965 ; Rifkin et al . , 1966 ] and of sheep [ Beale et al . , 1966 ] have not been established in detail ; the position of the amino - acid residues has ...
... sequence has not been established . The amino - acid sequence of mouse [ Popp , 1965 ; Rifkin et al . , 1966 ] and of sheep [ Beale et al . , 1966 ] have not been established in detail ; the position of the amino - acid residues has ...
Seite 330
These sequence studies have shown that the COOH - terminal half of either κ or λ light chains is invariant [ Hilschmann & Craig , 1965 ] , whereas several amino - acid interchanges have been shown in the NH2 - terminal half . One amino ...
These sequence studies have shown that the COOH - terminal half of either κ or λ light chains is invariant [ Hilschmann & Craig , 1965 ] , whereas several amino - acid interchanges have been shown in the NH2 - terminal half . One amino ...
Seite 333
... sequences of the light chains are reproduced from Fig . 6 ( see the legend to this figure for references ) . The amino - acid sequence of X chains is taken from Milstein [ 1966 ] , Hood et al . [ 1967 ] , Baglioni [ 1967 ] , and ...
... sequences of the light chains are reproduced from Fig . 6 ( see the legend to this figure for references ) . The amino - acid sequence of X chains is taken from Milstein [ 1966 ] , Hood et al . [ 1967 ] , Baglioni [ 1967 ] , and ...
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