Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 171
THE POSSIBLE ENZYMIC BASIS OF THE BIOSYNTHESIS OF BLOOD - GROUP SUBSTANCES WINIFRED M. WATKINS Lister Institute of Preventive Medicine , London , S.W.1 , England Blood - gre lood - group characters have for many years been widely used ...
THE POSSIBLE ENZYMIC BASIS OF THE BIOSYNTHESIS OF BLOOD - GROUP SUBSTANCES WINIFRED M. WATKINS Lister Institute of Preventive Medicine , London , S.W.1 , England Blood - gre lood - group characters have for many years been widely used ...
Seite 196
... blood of subjects with acatalas ( em ) ia . Their experiments with partially purified blood catalase ( Herbert - Pinsent method stage 2 or 3 ) , in particular its reactivity against anti - human blood - catalase serum , favor the ...
... blood of subjects with acatalas ( em ) ia . Their experiments with partially purified blood catalase ( Herbert - Pinsent method stage 2 or 3 ) , in particular its reactivity against anti - human blood - catalase serum , favor the ...
Seite 489
... blood typing was carried out by the Blood Bank of Hawaii under the Office of the Civil Defense . Nearly all children of school age on the island of Oahu were typed , as well as civilians in the school area . This excep- tional body of ...
... blood typing was carried out by the Blood Bank of Hawaii under the Office of the Civil Defense . Nearly all children of school age on the island of Oahu were typed , as well as civilians in the school area . This excep- tional body of ...
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