Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 98
... children already affected ) , microcephalic imbecility ( already two affected children ) , Krabbe's type of globoid cell leucodystrophy ( child dead ) , galactosemia , diaphysial aclasia ( father and one child affected ) , congenital ...
... children already affected ) , microcephalic imbecility ( already two affected children ) , Krabbe's type of globoid cell leucodystrophy ( child dead ) , galactosemia , diaphysial aclasia ( father and one child affected ) , congenital ...
Seite 99
... children each . Of these , who were deterred and so did not plan 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 ) ...
... children each . Of these , who were deterred and so did not plan 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 ) ...
Seite 468
... children ever born . As indicated in Table 2 , there are four types of families according to which child is present or absent . Families of types 2 and 3 with one child missing ( either the first or the second ) , cannot be ...
... children ever born . As indicated in Table 2 , there are four types of families according to which child is present or absent . Families of types 2 and 3 with one child missing ( either the first or the second ) , cannot be ...
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