Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 138
... recent review of the literature , Berger [ 7 ] showed that Ph1 was present in 256 cases out of a total 307 cases . The cases with no Ph1 include however childhood and atypi- cal leukemias as well as genuine cases of chronic myelogenous ...
... recent review of the literature , Berger [ 7 ] showed that Ph1 was present in 256 cases out of a total 307 cases . The cases with no Ph1 include however childhood and atypi- cal leukemias as well as genuine cases of chronic myelogenous ...
Seite 144
... recent observations show that patients previously exposed to X - rays and having developed chronic myelo- genous leukemia are carriers of the Ph ' [ 16 , 22 ] . Engel et al . [ 13 ] reported on a patient in whom chronic myelogenous ...
... recent observations show that patients previously exposed to X - rays and having developed chronic myelo- genous leukemia are carriers of the Ph ' [ 16 , 22 ] . Engel et al . [ 13 ] reported on a patient in whom chronic myelogenous ...
Seite 309
... recent interest in the feasibility of deriving follow - up histories of individuals , on a large scale , through the ... recently has the statistical value of such information been recognized , espe- cially as relating to the whole ...
... recent interest in the feasibility of deriving follow - up histories of individuals , on a large scale , through the ... recently has the statistical value of such information been recognized , espe- cially as relating to the whole ...
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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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