Search Results - Cohn, Dan
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Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation by Shapiro, Jay R, Lietman, Caressa, Grover, Monica, Lu, James T, Nagamani, Sandesh CS, Dawson, Brian C, Baldridge, Dustin M, Bainbridge, Matthew N, Cohn, Dan H, Blazo, Maria, Roberts, Timothy T, Brennen, Feng-Shu, Wu, Yimei, Gibbs, Richard A, Melvin, Pamela, Campeau, Philippe M, Lee, Brendan H
Published 2013Text -
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Next-generation sequencing for disorders of low and high bone mineral density by Sule, Gautam, Campeau, Philippe M., Zhang, Victor Wei, Nagamani, Sandesh C.S., Dawson, Brian C., Grover, Monica, Bacino, Carlos A., Sutton, V. Reid, Brunetti-Pierri, Nicola, Lu, James T., Lemire, Edmond, Gibbs, Richard A., Cohn, Dan H., Cui, Hong, Wong, Lee-Jun C., Lee, Brendan H.
Published 2013Text -
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Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with “Corner Fractures” by Lee, Chae Syng, Fu, He, Baratang, Nissan, Rousseau, Justine, Kumra, Heena, Sutton, V. Reid, Niceta, Marcello, Ciolfi, Andrea, Yamamoto, Guilherme, Bertola, Débora, Marcelis, Carlo L., Lugtenberg, Dorien, Bartuli, Andrea, Kim, Choel, Hoover-Fong, Julie, Sobreira, Nara, Pauli, Richard, Bacino, Carlos, Krakow, Deborah, Parboosingh, Jillian, Yap, Patrick, Kariminejad, Ariana, McDonald, Marie T., Aracena, Mariana I., Lausch, Ekkehart, Unger, Sheila, Superti-Furga, Andrea, Lu, James T., Cohn, Dan H., Tartaglia, Marco, Lee, Brendan H., Reinhardt, Dieter P., Campeau, Philippe M.
Published 2017Text