Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 218
... antigenic differences can similarly be detected between hemoglobins A and B , which differ in having glycine and arginine respectively at the 16th position of the delta chain [ Jones et al . , 1965 ] . The difference between ...
... antigenic differences can similarly be detected between hemoglobins A and B , which differ in having glycine and arginine respectively at the 16th position of the delta chain [ Jones et al . , 1965 ] . The difference between ...
Seite 220
... antigenic site than just the single sugar , and some evidence suggests that at least six or seven sugar residues may be important in an antigenic site [ Kabat , 1966 ] . If both of these fucoses are attached to the same molecule , a new ...
... antigenic site than just the single sugar , and some evidence suggests that at least six or seven sugar residues may be important in an antigenic site [ Kabat , 1966 ] . If both of these fucoses are attached to the same molecule , a new ...
Seite 235
... antigenic in C57 mice and highly antigenic in CBA mice ; this result was almost opposite to that obtained with ( T , G ) -A - L . Thus , substituting histidine for tyrosine in the antigenic site of two simple molecules of the same ...
... antigenic in C57 mice and highly antigenic in CBA mice ; this result was almost opposite to that obtained with ( T , G ) -A - L . Thus , substituting histidine for tyrosine in the antigenic site of two simple molecules of the same ...
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