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Browsing by Author "Topic, V. (57224327167)"

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    Publication
    Molecular analysis of ring y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency
    (2011)
    Milenkovic, T. (55889872600)
    ;
    Guc-Scekic, M. (6602359789)
    ;
    Zdravkovic, D. (7004544358)
    ;
    Topic, V. (57224327167)
    ;
    Liehr, T. (56404741200)
    ;
    Joksic, G. (6603704157)
    ;
    Radivojevic, D. (12769357500)
    ;
    Lakic, N. (35386377100)
    Ring Y chromosome is a very rare chromosomal aberration. The published mixed gonadal dysgenesis (MGD) patients with a ring Y chromosome are short in stature, but are not growth hormone (GH) deficient. We present the molecular cytogenetic and molecular characterization of ring Y chromosome mosaicism in a 10-year-old boy with MGD whose short stature could be explained by the high percentage of cells monosomic for the X-chromosome, but also by the presence of severe GH deficiency. The ring Y chromosome in our patient is a de novo structural aberration. The father's karyotype was normal.
  • Loading...
    Thumbnail Image
    Some of the metrics are blocked by your 
    consent settings
    Publication
    Molecular analysis of ring y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency
    (2011)
    Milenkovic, T. (55889872600)
    ;
    Guc-Scekic, M. (6602359789)
    ;
    Zdravkovic, D. (7004544358)
    ;
    Topic, V. (57224327167)
    ;
    Liehr, T. (56404741200)
    ;
    Joksic, G. (6603704157)
    ;
    Radivojevic, D. (12769357500)
    ;
    Lakic, N. (35386377100)
    Ring Y chromosome is a very rare chromosomal aberration. The published mixed gonadal dysgenesis (MGD) patients with a ring Y chromosome are short in stature, but are not growth hormone (GH) deficient. We present the molecular cytogenetic and molecular characterization of ring Y chromosome mosaicism in a 10-year-old boy with MGD whose short stature could be explained by the high percentage of cells monosomic for the X-chromosome, but also by the presence of severe GH deficiency. The ring Y chromosome in our patient is a de novo structural aberration. The father's karyotype was normal.

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