Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 116
... complex pattern of manifestation . It is thought that topogenetic correlations in organogenesis , reparation , and regulation processes have modified and varied the primary terato- genic disturbance . Hence the symptom is the result of ...
... complex pattern of manifestation . It is thought that topogenetic correlations in organogenesis , reparation , and regulation processes have modified and varied the primary terato- genic disturbance . Hence the symptom is the result of ...
Seite 224
... complex sero- logical systems is by biochemical analysis of the gene product . There are four instances in which apparent recombination has been reported in complex blood - group systems . Scheinberg [ 1956 ] has reported two cases in ...
... complex sero- logical systems is by biochemical analysis of the gene product . There are four instances in which apparent recombination has been reported in complex blood - group systems . Scheinberg [ 1956 ] has reported two cases in ...
Seite 505
... complex . Another year after that , the complex should be in its final form and accumulation of results should begin . Allow- ing for one or two false starts , we hope the complex will have discovered about half- a - dozen new linkages ...
... complex . Another year after that , the complex should be in its final form and accumulation of results should begin . Allow- ing for one or two false starts , we hope the complex will have discovered about half- a - dozen new linkages ...
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