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Elsevier, European Journal of Medical Genetics, 2(55), p. 103-108, 2012

DOI: 10.1016/j.ejmg.2011.11.003

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Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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