Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 95
... Further , the cost is often very great , necessitating subsidy and imposing administrative needs for efficiency . RESEARCH AND EDUCATION Development of uniform procedures in the collection of case material and pooling of the information ...
... Further , the cost is often very great , necessitating subsidy and imposing administrative needs for efficiency . RESEARCH AND EDUCATION Development of uniform procedures in the collection of case material and pooling of the information ...
Seite 98
... further children , whereas seventy - one , that is three - quarters , of the low risk group were prepared to accept the risk . It is perhaps surprising that as many as twenty - four should be undeterred by a high risk ( in eleven of ...
... further children , whereas seventy - one , that is three - quarters , of the low risk group were prepared to accept the risk . It is perhaps surprising that as many as twenty - four should be undeterred by a high risk ( in eleven of ...
Seite 99
... further children , about 1 in 7 had another child as a result of contraceptive failures , and one couple had two further children . The total fertility ( shown in Table 3 ) of the high risk group was 0.45 and of the low group 0.85 ...
... further children , about 1 in 7 had another child as a result of contraceptive failures , and one couple had two further children . The total fertility ( shown in Table 3 ) of the high risk group was 0.45 and of the low group 0.85 ...
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