Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 250
... frequency of any heterozygote AA , is 2pip ; ( 1 − F ) , and the frequency of any homozygote A¡A ; is p2 ( 1 − F ) + p.F. For m alleles this requires m - 1 independ- ent gene frequencies and the inbreeding coefficient , or m ...
... frequency of any heterozygote AA , is 2pip ; ( 1 − F ) , and the frequency of any homozygote A¡A ; is p2 ( 1 − F ) + p.F. For m alleles this requires m - 1 independ- ent gene frequencies and the inbreeding coefficient , or m ...
Seite 280
... frequencies among the colonies about the mean of the frequency for the sect is shown in Figs . 3 and 4 , for the S - leut and the L - leut , respectively . Equally great differences are shown by the frequencies for the ABO , Rh , and ...
... frequencies among the colonies about the mean of the frequency for the sect is shown in Figs . 3 and 4 , for the S - leut and the L - leut , respectively . Equally great differences are shown by the frequencies for the ABO , Rh , and ...
Seite 442
... frequency of the anomaly under random mating . Then in Fig . 6 , the frequencies in the population of children from first cousin marriages , corresponding to F = 16 , are compared with the respective p - values , under the ...
... frequency of the anomaly under random mating . Then in Fig . 6 , the frequencies in the population of children from first cousin marriages , corresponding to F = 16 , are compared with the respective p - values , under 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