Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 142
... reported in chronic as well as acute myelogenous leukemia [ 65 , 66 , 70 , 71 , 72 , 73 ] or in other hemopathies such as erythroleukemia [ 44 ] . b ) Solid Tumors . Most often the tumors that have been studied are well- established ...
... reported in chronic as well as acute myelogenous leukemia [ 65 , 66 , 70 , 71 , 72 , 73 ] or in other hemopathies such as erythroleukemia [ 44 ] . b ) Solid Tumors . Most often the tumors that have been studied are well- established ...
Seite 224
... reported in complex blood - group systems . Scheinberg [ 1956 ] has reported two cases in chickens in which the frequencies of recombination between determinants of cellular specifici- ties are 5.4 per cent and 2.6 per cent , high ...
... reported in complex blood - group systems . Scheinberg [ 1956 ] has reported two cases in chickens in which the frequencies of recombination between determinants of cellular specifici- ties are 5.4 per cent and 2.6 per cent , high ...
Seite 394
... reported . The heredity is irregular autosomal dominant . Sturge - Weber syndrome may be associated with Klippel - Trenaunay - Weber syndrome , and involvement of the hand may be explained by this combination . 4. Ataxia ...
... reported . The heredity is irregular autosomal dominant . Sturge - Weber syndrome may be associated with Klippel - Trenaunay - Weber syndrome , and involvement of the hand may be explained by this combination . 4. Ataxia ...
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