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Elsevier, European Journal of Medical Genetics, 2(63), p. 103657, 2020

DOI: 10.1016/j.ejmg.2019.04.014

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Compound heterozygous Pkd1l1 variants in a family with two fetuses affected by heterotaxy and complex Chd

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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