Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 213
... Locus PGM1 2 Locus PGM3 2 Placental alkaline phosphatase Acetyl transferase 2 Adenylate kinase 2 22322 0.58 0.47 0.53 0.50 0.41 0.31 0.50 0.50 0.90 0.82 Serum cholinesterase Locus E1 Locus E2 22 22 0.96 0.92 0.90 0.82 6 ...
... Locus PGM1 2 Locus PGM3 2 Placental alkaline phosphatase Acetyl transferase 2 Adenylate kinase 2 22322 0.58 0.47 0.53 0.50 0.41 0.31 0.50 0.50 0.90 0.82 Serum cholinesterase Locus E1 Locus E2 22 22 0.96 0.92 0.90 0.82 6 ...
Seite 231
... locus . Genetics 49 : 973 . 1965. The Ss system of the mouse - A quantitative serum protein difference genetically controlled by the H - 2 region . In Isoantigens and cell interactions , p . 11 . ed . J. PALM . Philadelphia : Wistar ...
... locus . Genetics 49 : 973 . 1965. The Ss system of the mouse - A quantitative serum protein difference genetically controlled by the H - 2 region . In Isoantigens and cell interactions , p . 11 . ed . J. PALM . Philadelphia : Wistar ...
Seite 346
... locus affecting IQ linked to a marker locus such as MN , which I choose since it has the advantage that we can recognize the heterozygote . To simplify the situation I postulate that the IQ locus has only two alleles of equal frequency ...
... locus affecting IQ linked to a marker locus such as MN , which I choose since it has the advantage that we can recognize the heterozygote . To simplify the situation I postulate that the IQ locus has only two alleles of equal frequency ...
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