Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 412
... X - chromosome is not observed during the mitosis of heterogametic male somatic cells ( XY ) . 2. During meiosis of the germ cells the heteropyknotic chromosome does not appear in the female germ cells . Neither of the two X - chromosomes ...
... X - chromosome is not observed during the mitosis of heterogametic male somatic cells ( XY ) . 2. During meiosis of the germ cells the heteropyknotic chromosome does not appear in the female germ cells . Neither of the two X - chromosomes ...
Seite 428
... X - chromosomes are required for normal development . The level of X - imbalance before this time depends on the ... chromosome in the early zygote and from the variation in the timing of inactivation from tissue to tissue rather than ...
... X - chromosomes are required for normal development . The level of X - imbalance before this time depends on the ... chromosome in the early zygote and from the variation in the timing of inactivation from tissue to tissue rather than ...
Seite 433
... X - chromosome . Lancet 2 : 434 . 1962. Sex chromatin and gene action in the mammalian X - chromosome . Amer . J. Hum . Genet . 14 : 135-48 . 1963. Attempts to test the inactive X - theory of dosage compensation in mam- mals . Genet ...
... X - chromosome . Lancet 2 : 434 . 1962. Sex chromatin and gene action in the mammalian X - chromosome . Amer . J. Hum . Genet . 14 : 135-48 . 1963. Attempts to test the inactive X - theory of dosage compensation in mam- mals . Genet ...
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