Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 125
... studies in animal 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 ] ...
... studies in animal 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 ] ...
Seite 148
... studies in four cases . Brit . Med . J. 1 : 1275 . 38. HUNGERFORD , D. A. & NOWELL , P. C. 1962. Chromosome studies in human leukaemia . III . Acute granulocytic leukaemia . J. Nat . Cancer Inst . 29 : 545 . 39. ISHIHARA , T. , MOORE ...
... studies in four cases . Brit . Med . J. 1 : 1275 . 38. HUNGERFORD , D. A. & NOWELL , P. C. 1962. Chromosome studies in human leukaemia . III . Acute granulocytic leukaemia . J. Nat . Cancer Inst . 29 : 545 . 39. ISHIHARA , T. , MOORE ...
Seite 292
... studies could also be incorporated into the family histories by the same methods , if there were reason to do so , but currently this is being avoided in order to focus our efforts on the main objectives . To date , a total of ten years ...
... studies could also be incorporated into the family histories by the same methods , if there were reason to do so , but currently this is being avoided in order to focus our efforts on the main objectives . To date , a total of ten years ...
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