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Elsevier, European Journal of Medical Genetics, 4(63), p. 103772, 2020

DOI: 10.1016/j.ejmg.2019.103772

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Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings

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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