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A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9

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Summary

A girl with 46, XX, del (11) (q23), inv (9) (p13,q13) is described. The patient shows many dysplastic signs mainly of the face and skull. The pericentric inversion of chromosome 9 has been inherited from the mother (46, XX, inv (9) (p13,q13)).

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References

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Authors and Affiliations

  1. Institut für Humangenetik der Universität Marburg, Marburg, Germany

    Bernhard Zabel, Susanne Hansen, Ulrike Hillig & Helga Gröting-Imhof

  2. DRK-Kinderklinik Siegen, Siegen, Germany

    Bernhard Zabel, Susanne Hansen, Ulrike Hillig & Helga Gröting-Imhof

Authors
  1. Bernhard Zabel
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  2. Susanne Hansen
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  3. Ulrike Hillig
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  4. Helga Gröting-Imhof
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Zabel, B., Hansen, S., Hillig, U. et al. A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9. Hum Genet 36, 117–122 (1977). https://doi.org/10.1007/BF00390443

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  • DOI: https://doi.org/10.1007/BF00390443

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