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Wiley, Clinical Genetics, p. n/a-n/a

DOI: 10.1111/cge.12771

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Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis

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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