Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 17
... problems , however , remained ; for exam- ple , how best to establish that segregation ratios , which were found in human families , were really Mendelian ? This problem could be treated in a great variety of ways according to the ...
... problems , however , remained ; for exam- ple , how best to establish that segregation ratios , which were found in human families , were really Mendelian ? This problem could be treated in a great variety of ways according to the ...
Seite 294
most biologists would regard the problems that confront them as being every bit as important as those of the nuclear physicists . Moreover , to some geneticists , the future of the human gene pool presents long - range problems that ...
most biologists would regard the problems that confront them as being every bit as important as those of the nuclear physicists . Moreover , to some geneticists , the future of the human gene pool presents long - range problems that ...
Seite 473
... problems encountered . The simulation of a population is therefore likely to become a frequent exercise , but the nature of the artificial population will certainly differ greatly every time . Our problems were so far mainly those of ...
... problems encountered . The simulation of a population is therefore likely to become a frequent exercise , but the nature of the artificial population will certainly differ greatly every time . Our problems were so far mainly those 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