Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 120
... Down's syndrome ( Mongolism ) with normal chromosomes . Lancet ii : 1026 . 43. ZELLWEGER , H. , & Abbo , G. 1964. Moderne Mongolismus - Probleme . Dtsch . med . Wschr . 89 : 405 . 44. FITZGERALD , P. H. & LYCETTE , R. R. 1961. Mosaicism ...
... Down's syndrome ( Mongolism ) with normal chromosomes . Lancet ii : 1026 . 43. ZELLWEGER , H. , & Abbo , G. 1964. Moderne Mongolismus - Probleme . Dtsch . med . Wschr . 89 : 405 . 44. FITZGERALD , P. H. & LYCETTE , R. R. 1961. Mosaicism ...
Seite 509
... Down's syndrome was never convincing . It did not fit several facts concerning the abnormality , particularly those derived from studies on twins . Many twin pairs in which Down's syndrome occurs are concordant , i.e. , both twins are ...
... Down's syndrome was never convincing . It did not fit several facts concerning the abnormality , particularly those derived from studies on twins . Many twin pairs in which Down's syndrome occurs are concordant , i.e. , both twins are ...
Seite 510
... 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 after fertilization of a chromosomally normal egg ...
... 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 after fertilization of a chromosomally normal egg ...
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