Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 146
... specific suggests that it obeys certain laws . Some of these have been proposed by Lejeune [ 48 ] . One is the duplication of normal or abnormal super- numerary chromosomes . A second one is that the karyotype upsetting is kept from ...
... specific suggests that it obeys certain laws . Some of these have been proposed by Lejeune [ 48 ] . One is the duplication of normal or abnormal super- numerary chromosomes . A second one is that the karyotype upsetting is kept from ...
Seite 184
... specific transfer of N - acetyl- galactosamine to hog H substance using a mixture of C1 - labeled uridine diphosphate N - acetylhexosamines as the sugar donor and hog gastric mucosal linings as a source of the A gene - specified N ...
... specific transfer of N - acetyl- galactosamine to hog H substance using a mixture of C1 - labeled uridine diphosphate N - acetylhexosamines as the sugar donor and hog gastric mucosal linings as a source of the A gene - specified N ...
Seite 513
... specific gene in the X - chromosome . Many human traits do not fall into two or a few alternative classes as those just mentioned . Or , even if they do , pedigrees fail to yield the proportions expected from simple genetic situations ...
... specific gene in the X - chromosome . Many human traits do not fall into two or a few alternative classes as those just mentioned . Or , even if they do , pedigrees fail to yield the proportions expected from simple genetic situations ...
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