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A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation

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References

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Authors and Affiliations

  1. National University Health System, 1E Kent Ridge Rd, Singapore, 119228, Singapore

    Ai Peng Tan

  2. Great Ormond Street Hospital NHS Foundation Trust, Great Ormond St, London, WC1N 3JH, UK

    Kshitij Mankad

Authors
  1. Ai Peng Tan
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  2. Kshitij Mankad
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Correspondence to Ai Peng Tan.

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Tan, A.P., Mankad, K. A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation. Childs Nerv Syst 34, 23–25 (2018). https://doi.org/10.1007/s00381-017-3646-0

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  • DOI: https://doi.org/10.1007/s00381-017-3646-0

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