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Original research
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals

Authors

  1. Correspondence to Dr Saskia Koene, Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands; s.koene{at}lumc.nl
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Citation

Koene S, Ropers FG, Wieland J, et al
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals

Publication history

  • Received July 26, 2023
  • Accepted November 21, 2023
  • First published December 16, 2023.
Online issue publication 
March 21, 2024

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