Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 65
them , little is known about structural variation in the proteins . Some proteins are known to be deficient in more than one genetic disease ( e.g. , antihemophilic globulin or factor VIII is diminished both in hemophilia and in Von ...
them , little is known about structural variation in the proteins . Some proteins are known to be deficient in more than one genetic disease ( e.g. , antihemophilic globulin or factor VIII is diminished both in hemophilia and in Von ...
Seite 144
... known for their carcinogenic properties are also liable to induce chromosome aberrations that share many features with those aberra- tions described in neoplasia . Yet other factors , nonexternal ones , may also be respon- sible for the ...
... known for their carcinogenic properties are also liable to induce chromosome aberrations that share many features with those aberra- tions described in neoplasia . Yet other factors , nonexternal ones , may also be respon- sible for the ...
Seite 318
... known about this protein . = There are at least four different hemoglobins ( Hb ) in man , each consisting of two ... known [ Ingram , 1963 ; Jones , 1964 ] ; nothing is known on the e chain , which is found in small embryos only ...
... known about this protein . = There are at least four different hemoglobins ( Hb ) in man , each consisting of two ... known [ Ingram , 1963 ; Jones , 1964 ] ; nothing is known on the e chain , which is found in small embryos only ...
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