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A new camptodactyly syndrome
  1. M Baraitser
  1. Clinical Genetics Unit, The Hospital for Sick Children, Great Ormond Street, London

    Abstract

    A family is reported in which scoliosis and camptodactyly occurred in members over four generations. Additional features were torticollis, fusion of cervical vertebrae, and occasional limitation of joint movement in the upper limbs. Inheritance is autosomal dominant.

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