Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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... involved in the matings mentioned above and computing F for these new sets . Pairing of each male with each female in the sect would have involved over 800,000 pairings . Not only is this a formidable task , even with a computer , but ...
... involved in the matings mentioned above and computing F for these new sets . Pairing of each male with each female in the sect would have involved over 800,000 pairings . Not only is this a formidable task , even with a computer , but ...
Seite 295
... involved than would agreement of the much rarer initial Z ( for Zacharias ) . The weight to be assigned to any such agreement or disagreement of any item of identify- ing information can fortunately be computed quite simply using ...
... involved than would agreement of the much rarer initial Z ( for Zacharias ) . The weight to be assigned to any such agreement or disagreement of any item of identify- ing information can fortunately be computed quite simply using ...
Seite 344
... involved . Using the same principles we [ Thoday , Gib- son , & Spickett , 1964 ; Spickett & Thoday , 1966 ; Gibson & Thoday , 1962 ; Wolsten- holme & Thoday , 1963 ] have analyzed a number of high sternopleural chaeta number lines of ...
... involved . Using the same principles we [ Thoday , Gib- son , & Spickett , 1964 ; Spickett & Thoday , 1966 ; Gibson & Thoday , 1962 ; Wolsten- holme & Thoday , 1963 ] have analyzed a number of high sternopleural chaeta number lines of ...
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