Stuart, B. D. Et Al. 2015. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening. NATURE GENETICS , vol.47, no.5 , 512-517.

Stuart, B. D., Choi, J., Zaidi, S., Xing, C., Holohan, B., Chen, R., ... Choi, M.(2015). Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening. NATURE GENETICS , vol.47, no.5, 512-517.

Stuart, Bridget Et Al. "Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening," NATURE GENETICS , vol.47, no.5, 512-517, 2015

Stuart, Bridget D. Et Al. "Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening." NATURE GENETICS , vol.47, no.5, pp.512-517, 2015

Stuart, B. D. Et Al. (2015) . "Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening." NATURE GENETICS , vol.47, no.5, pp.512-517.

@article{article, author={Bridget D. Stuart Et Al. }, title={Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening}, journal={NATURE GENETICS}, year=2015, pages={512-517} }