Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
Im Buch
Ergebnisse 1-3 von 89
Seite 125
... cells by Lima de Faria followed soon afterwards [ 18 , 19 ] . The first report of mammalian cell studies was made by Taylor in 1960 [ 28 ] , and the first report of a human cell study was read in the spring of 1961 [ 7 ] . In 1961 ...
... cells by Lima de Faria followed soon afterwards [ 18 , 19 ] . The first report of mammalian cell studies was made by Taylor in 1960 [ 28 ] , and the first report of a human cell study was read in the spring of 1961 [ 7 ] . In 1961 ...
Seite 130
... cells , there may be an example of activation of only one of two homologous chromosomal regions : in multiple myeloma it has been demonstrated that a large number of cells , possibly a clone , engaged in the production of a single ...
... cells , there may be an example of activation of only one of two homologous chromosomal regions : in multiple myeloma it has been demonstrated that a large number of cells , possibly a clone , engaged in the production of a single ...
Seite 425
... cells . 5. Simultaneous addition of small amounts of NaNO2 , glucose , and methylene blue to normal red cells gives a maximum methemoglobin formation after one hour incubation [ Tönz , 1965 ] , while after four hours nearly all ...
... cells . 5. Simultaneous addition of small amounts of NaNO2 , glucose , and methylene blue to normal red cells gives a maximum methemoglobin formation after one hour incubation [ Tönz , 1965 ] , while after four hours nearly all ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
35 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
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