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Author/Creator Finn, Erin

1. A Novel Intronic Pathogenic Variant in STAR With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal Hyperplasia. (May 2021)

Authors:
Finn, Erin; Kripps, Kimberly; Chambers, Christina; Rapp, Michele; Meeks, Naomi J. L.; Xu, Fang; Chen, Wuyan; Larson, Austin A.; Nokoff, Natalie J.
Journal:
Journal of investigative medicine high impact case reports
Issue:
Volume 9(2021)
Page Start:
Record Type:
Journal Article
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3. EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features. Issue 5 (4th June 2015)

Authors:
Ganetzky, Rebecca; Finn, Erin; Bagchi, Atrish; Zollo, Ornella; Conlin, Laura; Deardorff, Matthew; Harr, Margaret; Simpson, Michael A.; McGrath, John A.; Zackai, Elaine; Lemmon, Mark A.; Sondheimer, Neal
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 3:Issue 5(2015:Sep.)
Page Start:
452
Record Type:
Journal Article
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4. Fracture fixation in the operative management of hip fractures (FAITH): an international, multicentre, randomised controlled trial. Issue 10078 (15th April 2017)

Authors:
Nauth, Aaron; Creek, Aaron T.; Zellar, Abby; Lawendy, Abdel-Rahman; Dowrick, Adam; Gupta, Ajay; Dadi, Akhil; van Kampen, Albert; Yee, Albert; de Vries, Alexander C.; de Mol van Otterloo, Alexander; Garibaldi, Alisha; Liew, Allen; McIntyre, Allison W.; Prasad, Amal Shankar; Romero, Amanda W.; Rang...
Journal:
Lancet
Issue:
Volume 389:Issue 10078(2017)
Page Start:
1519
Record Type:
Journal Article
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