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Roberts syndrome: clinical and cytogenetic aspects
  1. N P Mann,
  2. J Fitzsimmons,
  3. E Fitzsimmons,
  4. P Cooke
  1. 1Clinical Genetic Service, City Hospital, Nottingham NG5 1PB

    Abstract

    Roberts syndrome is reported in two sibs of consanguineous parents. Both infants had severe tetraphocomelia, facial clefting, and other serious malformations. In addition they were found to have an unusual cytogenetic abnormality with distortion of the normal sister chromatid relationship in many chromosomes.

    https://doi.org/10.1136/jmg.19.2.116

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