檢索結果 - Cohn, Dan

The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect 由 Tiemann-Boege, Irene, Navidi, William, Grewal, Raji, Cohn, Dan, Eskenazi, Brenda, Wyrobek, Andrew J., Arnheim, Norman

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Disease Gene Characterization through Large-Scale Co-Expression Analysis 由 Day, Allen, Dong, Jun, Funari, Vincent A., Harry, Bret, Strom, Samuel P., Cohn, Dan H., Nelson, Stanley F.

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Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation 由 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

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Next-generation sequencing for disorders of low and high bone mineral density 由 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.

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Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with “Corner Fractures” 由 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.

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