Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 123
... abnormalities of sex chromosomes . Spontaneously aborted fetuses have been shown to have numerical chromosomal abnormalities in 20-25 per cent of cases . Genetic imbal- ance , the result of structural rearrangements of chromosomes , has ...
... abnormalities of sex chromosomes . Spontaneously aborted fetuses have been shown to have numerical chromosomal abnormalities in 20-25 per cent of cases . Genetic imbal- ance , the result of structural rearrangements of chromosomes , has ...
Seite 149
... Chromosomal abnormalities in leukaemias . Lancet 2 : 589 . 71. Ruffie , J. , Ducos , J. , BIErme , R. , ColomBIES , P. , & SALLES - Mourlan , A. M. 1965. Multiple chromosomal abnormalities in an acute exacerbation of myeloid leukaemia ...
... Chromosomal abnormalities in leukaemias . Lancet 2 : 589 . 71. Ruffie , J. , Ducos , J. , BIErme , R. , ColomBIES , P. , & SALLES - Mourlan , A. M. 1965. Multiple chromosomal abnormalities in an acute exacerbation of myeloid leukaemia ...
Seite 428
... chromosomal abnormalities the largest group is represented by XO fetuses , is interesting [ Hirschhorn & Firschein , 1964 ] . Lyon [ 1963 ] remarks that there is no positive evidence in favor of the hypothesis of Gartler and Sparkes ...
... chromosomal abnormalities the largest group is represented by XO fetuses , is interesting [ Hirschhorn & Firschein , 1964 ] . Lyon [ 1963 ] remarks that there is no positive evidence in favor of the hypothesis of Gartler and Sparkes ...
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