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Microcephaly-cardiomyopathy: a new autosomal recessive phenotype?
  1. I M Winship,
  2. D L Viljoen,
  3. P M Leary,
  4. M M De Moor
  1. Department of Human Genetics, University of Cape Town Medical School, Observatory, South Africa.

    Abstract

    A distinctive phenotype of severe microcephaly and self-limiting dilated cardiomyopathy has been observed in two sibs suggesting autosomal recessive inheritance. Mental retardation, delayed developmental milestones, and minor dysmorphism were additional features.

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