Cite
HARVARD Citation
Grandone, A. et al. (2016). Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis. Clinical genetics. 90 (5), pp. 445-450. [Online].
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Grandone, A. et al. (2016). Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis. Clinical genetics. 90 (5), pp. 445-450. [Online].