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A case which further refines the critical region for 15q25.2 microduplication phenotypes

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Authors and Affiliations

  1. Génétique médicale, Université d’Auvergne, Centre hospitalo-universitaire de Clermont-Ferrand, Clermont-Ferrand, France

    Cécile Yossa Monkam, Anne Miret & Catherine Sarret

  2. Cytogénétique médicale, Université d’Auvergne, Centre hospitalo-universitaire de Clermont-Ferrand, Clermont-Ferrand, France

    Stéphan Kemeny & Céline Pebrel-Richard

  3. IGCNC, EA7282, Université d’Auvergne, Clermont-Ferrand, France

    Catherine Sarret

Authors
  1. Cécile Yossa Monkam
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  2. Stéphan Kemeny
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  3. Anne Miret
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  4. Céline Pebrel-Richard
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  5. Catherine Sarret
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Corresponding author

Correspondence to Catherine Sarret.

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The authors declare no conflict of interest. All contributing authors have consented to publication.

Ethical approval

This study was approved by our local Institutional review board.

Informed consent

Written informed consent was obtained from the child's parents for genetic analyses and publication of photographies.

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Monkam, C.Y., Kemeny, S., Miret, A. et al. A case which further refines the critical region for 15q25.2 microduplication phenotypes. Acta Neurol Belg 116, 683–685 (2016). https://doi.org/10.1007/s13760-016-0620-7

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  • DOI: https://doi.org/10.1007/s13760-016-0620-7

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