Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 126
... example of the converse , homologue asynchrony , is to be found in the X's of the female ( XX ) cell , but autosomal regions also may show it . There has been much interest in the X asynchrony but relatively little in autosomal ...
... example of the converse , homologue asynchrony , is to be found in the X's of the female ( XX ) cell , but autosomal regions also may show it . There has been much interest in the X asynchrony but relatively little in autosomal ...
Seite 212
... example the precise nature of the structural differences between the variant forms of a given enzyme and whether these are reflected in functional differences . It is interesting to note that in five of the polymorphisms listed in Table ...
... example the precise nature of the structural differences between the variant forms of a given enzyme and whether these are reflected in functional differences . It is interesting to note that in five of the polymorphisms listed in Table ...
Seite 296
... examples . The searching step can likewise be made efficient by the application of some fairly simple mathematical principles . The file sequence , for example , should be based on those components of the identifying information that ...
... examples . The searching step can likewise be made efficient by the application of some fairly simple mathematical principles . The file sequence , for example , should be based on those components of the identifying information that ...
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