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Elsevier, European Journal of Medical Genetics, 8(61), p. 442-450

DOI: 10.1016/j.ejmg.2018.03.002

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Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia

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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