Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite xvii
... human isolate Arthur G. Steinberg , Hermann K. Bleibtreu , Thaddeus W. Kurczynski , Alice O. Martin , and Elizabeth ... HUMAN EVOLUTION New insights into continuous variation J. M. Thoday Human evolution and ecology G. Ainsworth Harrison ...
... human isolate Arthur G. Steinberg , Hermann K. Bleibtreu , Thaddeus W. Kurczynski , Alice O. Martin , and Elizabeth ... HUMAN EVOLUTION New insights into continuous variation J. M. Thoday Human evolution and ecology G. Ainsworth Harrison ...
Seite 56
... human and sheep insulin . Amer . J. Med . 40 : 652 . 28. MERRIFIELD , R. B. 1965. Automated synthesis of peptides . Science 150 : 178 . 29. DEMARS , R. 1965. Investigations in human genetics with cultivated human cells : a summary of ...
... human and sheep insulin . Amer . J. Med . 40 : 652 . 28. MERRIFIELD , R. B. 1965. Automated synthesis of peptides . Science 150 : 178 . 29. DEMARS , R. 1965. Investigations in human genetics with cultivated human cells : a summary of ...
Seite 339
... human genetic studies lay both at the foundation and the fringe of the main streams of genetic development . They lay at the foundation because our interest in individual humans leads to inten- sive study especially of rare pathologies ...
... human genetic studies lay both at the foundation and the fringe of the main streams of genetic development . They lay at the foundation because our interest in individual humans leads to inten- sive study especially of rare pathologies ...
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