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1. Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome-1 in two new patients with the same homozygous TMCO1 variant and review of the literature

   1. Abdelrazek, Ibrahim M.
   2. Holling, Tess
   3. Harms, Frederike Leonie
   4. Alawi, Malik
   5. Omar, Tarek
   6. Abdalla, Ebtesam
   7. Kutsche, Kerstin

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