Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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... effects of mutant alleles but not of the normal alleles . The problem has become acute because of the recognition in man of chromosomal aberrations in many of which , like the trisomies , there is an alteration in the number of normal ...
... effects of mutant alleles but not of the normal alleles . The problem has become acute because of the recognition in man of chromosomal aberrations in many of which , like the trisomies , there is an alteration in the number of normal ...
Seite 258
... effects on mortality and morbidity are largely due to rare genes ( idiomorphs ) maintained by mutation [ Mi et al . , 1965 ] . The Brazilian population is of long standing and there is little racial endogamy , the residual inbreeding ...
... effects on mortality and morbidity are largely due to rare genes ( idiomorphs ) maintained by mutation [ Mi et al . , 1965 ] . The Brazilian population is of long standing and there is little racial endogamy , the residual inbreeding ...
Seite 303
... effects ) Certain diseases of early infancy 760-776 58 2.16 10.6 Intracranial & spinal injury at birth 760 123a 1.80 9.1 Higher birth orders ( 3rd and over vs. 1st and 2nd ) ( excluding maternal age effects ) Infective & parasitic ...
... effects ) Certain diseases of early infancy 760-776 58 2.16 10.6 Intracranial & spinal injury at birth 760 123a 1.80 9.1 Higher birth orders ( 3rd and over vs. 1st and 2nd ) ( excluding maternal age effects ) Infective & parasitic ...
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