Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 78
... demonstrated in distinguishing between the double abnor- mality , Klinefelter - Mongolism , and the XXYY sex - chromosome complement where the cytological picture is not clear enough to identify the six small acrocentrics with certainty ...
... demonstrated in distinguishing between the double abnor- mality , Klinefelter - Mongolism , and the XXYY sex - chromosome complement where the cytological picture is not clear enough to identify the six small acrocentrics with certainty ...
Seite 156
... demonstrated the destruction of intestinal cells but the microvilli is equivalent to a " purification " of hydrolytic action by a factor of ten [ 68 ] . Otherwise , Doell and his coworkers , using an indirect fluorescent staining ...
... demonstrated the destruction of intestinal cells but the microvilli is equivalent to a " purification " of hydrolytic action by a factor of ten [ 68 ] . Otherwise , Doell and his coworkers , using an indirect fluorescent staining ...
Seite 218
... demonstrated for several cases in which the structural difference is established . Three different forms of human hemoglobin , A , S , and C , which differ by the presence at the sixth position of the beta chain of glutamic acid ...
... demonstrated for several cases in which the structural difference is established . Three different forms of human hemoglobin , A , S , and C , which differ by the presence at the sixth position of the beta chain of glutamic acid ...
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