Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 221
... single structural grouping which is genetically variable in its precise configuration . There is good evidence from studies of antisera against single haptens that a heterogeneous population of antibodies is produced , which can be ...
... single structural grouping which is genetically variable in its precise configuration . There is good evidence from studies of antisera against single haptens that a heterogeneous population of antibodies is produced , which can be ...
Seite 222
... single base pair at which a mutational change might determine a single antigenic amino - acid substitution in the protein product , or a segment of a locus such as that determining the specific substrate - binding site of an enzyme ...
... single base pair at which a mutational change might determine a single antigenic amino - acid substitution in the protein product , or a segment of a locus such as that determining the specific substrate - binding site of an enzyme ...
Seite 227
... single map with six subdivisions , as shown in Fig . 4. Following the suggestion of Snell et al . [ 1964 ] and Stimpfling and Richard- son [ 1965 ] , each of the subdivisions has been given a letter designation for easy reference . The ...
... single map with six subdivisions , as shown in Fig . 4. Following the suggestion of Snell et al . [ 1964 ] and Stimpfling and Richard- son [ 1965 ] , each of the subdivisions has been given a letter designation for easy reference . 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