Cite
HARVARD Citation
Suter, A. et al. (2016). Rothmund–Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene. Molecular genetics & genomic medicine. 4 (3), pp. 359-366. [Online].
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Suter, A. et al. (2016). Rothmund–Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene. Molecular genetics & genomic medicine. 4 (3), pp. 359-366. [Online].