Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 48
... increased requirement for the vitamin in the medium to support growth of the organism . These observations suggested ... increasing the oral intake of phosphorus ; no sup- plement of vitamin D may be needed to produce healing of bones ...
... increased requirement for the vitamin in the medium to support growth of the organism . These observations suggested ... increasing the oral intake of phosphorus ; no sup- plement of vitamin D may be needed to produce healing of bones ...
Seite 144
... increased by a factor of 20 when compared to normals . The type of leukemia is variable , acute myeloblastic , acute ... increased frequency of thyroid antibodies in mothers of trisomics 21 , and it has been suggested that maternal ...
... increased by a factor of 20 when compared to normals . The type of leukemia is variable , acute myeloblastic , acute ... increased frequency of thyroid antibodies in mothers of trisomics 21 , and it has been suggested that maternal ...
Seite 239
... INCREASED GAMMA GLOBULIN BRHEUMATOID FACTOR ANTIBODIES TO COLON BANTINUCLEAR FACTOR 4 5 5a 6 7 * OTHER ABNORMALITIES 8 9 10 11 I POSITIVE DIRECT COOMBS TEST 2 POLYARTERITIS NODOSA 3 THYROID ANTIBODIES 4 PANCARDITIS AND THYROTOXICOSIS 5 ...
... INCREASED GAMMA GLOBULIN BRHEUMATOID FACTOR ANTIBODIES TO COLON BANTINUCLEAR FACTOR 4 5 5a 6 7 * OTHER ABNORMALITIES 8 9 10 11 I POSITIVE DIRECT COOMBS TEST 2 POLYARTERITIS NODOSA 3 THYROID ANTIBODIES 4 PANCARDITIS AND THYROTOXICOSIS 5 ...
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