Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 227
... region because the informative crossovers have not yet been found , but they have been shown to lie in that part of the region delineated by the horizontal line . This map probably does not represent the limit of genetic resolution ...
... region because the informative crossovers have not yet been found , but they have been shown to lie in that part of the region delineated by the horizontal line . This map probably does not represent the limit of genetic resolution ...
Seite 228
... region is a finding of con- siderable interest . This location appears quite definite ; two pairs of recombinants are consistent in locating it at the same point . The significance of this position remains to be elucidated . It seems ...
... region is a finding of con- siderable interest . This location appears quite definite ; two pairs of recombinants are consistent in locating it at the same point . The significance of this position remains to be elucidated . It seems ...
Seite 229
... region to another . The high D - K frequency in H - 2 is suggestive of separate loci , but we certainly do not yet have enough information to warrant any firm conclusion . Those groups of specificities which have not been observed to ...
... region to another . The high D - K frequency in H - 2 is suggestive of separate loci , but we certainly do not yet have enough information to warrant any firm conclusion . Those groups of specificities which have not been observed to ...
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