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  • Title: [Pericentric inversions of chromosomes 1, 9 and 16 in patients with sex chromosome anomalies].
    Author: Verlinskaia DK, Prozorova MV, Khitrikov LE.
    Journal: Tsitol Genet; 1982; 16(1):57-60. PubMed ID: 7064223.
    Abstract:
    Studies on C-heterochromatin in chromosomes 1, 9, 16 in 83 patients with the Shereshevsky-Turner syndrome and in 23 patients with the Klinefelter syndrome revealed the highest number of inversions in chromosome 9 and no inversions in chromosome 16. The inversion frequency in chromosomes 1 and 9 did not significantly differ from the control. Complete inversions were found only in the patients with isochromosome Xq, their frequency being increased in this group. A significant rise of complete inversions in chromosome 9 was found in a group of patients with Klinefelter syndrome. A tendency to inversion concentrations in chromosome 9 under human autosome anomalies, reported in the literature, was also detected in patients with sex chromosome anomalies.
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