Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 254
... estimating F & T when p , FIT , FIs , and the distribution function of p ' are unknown . The error of the estimate cannot be determined . Even if a magician could tell us the value of FST , it would give no information about the ...
... estimating F & T when p , FIT , FIs , and the distribution function of p ' are unknown . The error of the estimate cannot be determined . Even if a magician could tell us the value of FST , it would give no information about the ...
Seite 255
... estimate was only FIT = .0226 , or 46 per cent of the value calculated from isonymy . The uncertain reliability of the isonymy calculation of FST must also be borne in mind . In these isolates most of the inbreeding coefficient estimated ...
... estimate was only FIT = .0226 , or 46 per cent of the value calculated from isonymy . The uncertain reliability of the isonymy calculation of FST must also be borne in mind . In these isolates most of the inbreeding coefficient estimated ...
Seite 262
... estimate may be made by noting that σ is the variance of parental distance along an axis , and with isotropic migration this is equal to 1⁄2 the variance of parental distance in the plane or marital distance along an axis and to 1⁄4 the ...
... estimate may be made by noting that σ is the variance of parental distance along an axis , and with isotropic migration this is equal to 1⁄2 the variance of parental distance in the plane or marital distance along an axis and to 1⁄4 the ...
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