Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 209
... occur in human populations . One would also like to know the answer to two further questions . The first is whether the enzyme polymorphisms that do occur are usually a matter of quantita- tive differences in rates of synthesis or ...
... occur in human populations . One would also like to know the answer to two further questions . The first is whether the enzyme polymorphisms that do occur are usually a matter of quantita- tive differences in rates of synthesis or ...
Seite 236
... occur in at least one first - degree relative of most subjects with acquired agammaglobulinemia [ 15 ] . These findings suggest that certain basic immunologic alterations occur in families of patients with acquired agammaglobulinemia ...
... occur in at least one first - degree relative of most subjects with acquired agammaglobulinemia [ 15 ] . These findings suggest that certain basic immunologic alterations occur in families of patients with acquired agammaglobulinemia ...
Seite 399
... occur and there may be palmar fascial contracture . The movements of the hand and fingers have been described as delicate or gracile [ 6 ] . The heredity is autosomal recessive . 4. Marchesani's syndrome includes brachymorphia with ...
... occur and there may be palmar fascial contracture . The movements of the hand and fingers have been described as delicate or gracile [ 6 ] . The heredity is autosomal recessive . 4. Marchesani's syndrome includes brachymorphia with ...
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