Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 125
... origin grown in tissue culture . Most of the information is from phyto- hemagglutinin - stimulated lymphocytes , and a few studies have employed skin- derived fibroblasts or aneuploid cells of neoplastic tissue origin . No detailed ...
... origin grown in tissue culture . Most of the information is from phyto- hemagglutinin - stimulated lymphocytes , and a few studies have employed skin- derived fibroblasts or aneuploid cells of neoplastic tissue origin . No detailed ...
Seite 333
... origin to the light - chain genes and further doubling gave origin to heavy - chain genes . A hypothetical evolutionary tree of the immunoglobulin genes is shown in Fig . 8. Similarities between heavy chains have not yet been proved by ...
... origin to the light - chain genes and further doubling gave origin to heavy - chain genes . A hypothetical evolutionary tree of the immunoglobulin genes is shown in Fig . 8. Similarities between heavy chains have not yet been proved by ...
Seite 510
... origin of the " 21 - trisomy " responsible for Down's syndrome . Whether this is indeed the true origin is unclear at present . There is evidence from mice that nondisjunction may occur not only prior to fertilization but also soon ...
... origin of the " 21 - trisomy " responsible for Down's syndrome . Whether this is indeed the true origin is unclear at present . There is evidence from mice that nondisjunction may occur not only prior to fertilization but also soon ...
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