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Monosomy 10qter: a new case.
  1. M Teyssier,
  2. C Charrin,
  3. J Dutruge,
  4. C Rousselle
  1. Laboratoire Central D'Hématologie et de Cytogénétique, Hôpital Edouard Herriot, Lyon, France.

    Abstract

    A new case of terminal deletion 10q26-qter is described. The phenotypic features are compatible with those of the previously reported cases. Deafness is reported for the first time.

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