Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 340
... Major gene variables may be considered as of two kinds . The pathological , whose study is both of clinical importance and also of fundamental importance in the same way as study of major variables has been in all organisms in giving us ...
... Major gene variables may be considered as of two kinds . The pathological , whose study is both of clinical importance and also of fundamental importance in the same way as study of major variables has been in all organisms in giving us ...
Seite 470
... major limitations of the data are that they relate only to a single generation and do not , in general , provide data on complete families . Nonresponse rates for individual data . items vary considerably with socioeconomic status and ...
... major limitations of the data are that they relate only to a single generation and do not , in general , provide data on complete families . Nonresponse rates for individual data . items vary considerably with socioeconomic status and ...
Seite 536
... major aims previously stressed . Persons who favor what they consider genetic improvement are of course all agreed on the major value of intelligence . However , they are far from agreed on the need for more cooperative- ness , and even ...
... major aims previously stressed . Persons who favor what they consider genetic improvement are of course all agreed on the major value of intelligence . However , they are far from agreed on the need for more cooperative- ness , and even ...
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