Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 280
... colonies within a sect are compared . The fre- quency of the M allele varied from 0.36 to 0.90 among the 44 S - leut colonies and from 0.49 to 0.84 among the 33 L - leut colonies . These frequencies are exceeded at the lower end only by ...
... colonies within a sect are compared . The fre- quency of the M allele varied from 0.36 to 0.90 among the 44 S - leut colonies and from 0.49 to 0.84 among the 33 L - leut colonies . These frequencies are exceeded at the lower end only by ...
Seite 281
... colonies which had been separated for less than five years at the time we examined them . Alternatively , we may con- sider the members of the new colonies as founder populations derived from the original one . A comparison of the gene ...
... colonies which had been separated for less than five years at the time we examined them . Alternatively , we may con- sider the members of the new colonies as founder populations derived from the original one . A comparison of the gene ...
Seite 285
... colonies consists of all those who lived in the colony at some time during the colony's existence . The sample for the estima- tion of blood type frequencies is composed of those members of the reconstituted colonies who survived and ...
... colonies consists of all those who lived in the colony at some time during the colony's existence . The sample for the estima- tion of blood type frequencies is composed of those members of the reconstituted colonies who survived and ...
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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Häufige Begriffe und Wortgruppen
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