Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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... patterns . The pattern in the Hela tissue culture cell line , aneuploid human female cells of malignant tissue origin , is different from that in diploid female cells in culture ; e.g. , the late - replicating X as well as many of the ...
... patterns . The pattern in the Hela tissue culture cell line , aneuploid human female cells of malignant tissue origin , is different from that in diploid female cells in culture ; e.g. , the late - replicating X as well as many of the ...
Seite 131
... pattern . These interesting cells with such a grain distribution have not been useful in the characterization of chromosomes , the objec- tive of most experiments , and it must be admitted that they are usually ignored or classified as ...
... pattern . These interesting cells with such a grain distribution have not been useful in the characterization of chromosomes , the objec- tive of most experiments , and it must be admitted that they are usually ignored or classified as ...
Seite 142
... pattern is the loss of a 21-22 , the duplication of the Ph1 and the acquisition of a 6–12 [ 28 ] . These general patterns are also suggested in acute leukemias . The series of myelo- blastic leukemias studied by Sandberg et al . [ 72 ...
... pattern is the loss of a 21-22 , the duplication of the Ph1 and the acquisition of a 6–12 [ 28 ] . These general patterns are also suggested in acute leukemias . The series of myelo- blastic leukemias studied by Sandberg et al . [ 72 ...
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