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	1.	Temperature-activated ion channels in neural crest cells confer maternal fever-associated birth defects. [electronic resource] by Hutson, Mary R Keyte, Anna L Hernández-Morales, Miriam Gibbs, Eric Kupchinsky, Zachary A Argyridis, Ioannis Erwin, Kyle N Pegram, Kelly Kneifel, Margaret Rosenberg, Paul B Matak, Pavle Xie, Luke Grandl, Jörg Davis, Erica E Katsanis, Nicholas Liu, Chunlei Benner, Eric J Producer: 20180530 In: Science signaling vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [electronic resource] by Shaw, Natalie D Brand, Harrison Kupchinsky, Zachary A Bengani, Hemant Plummer, Lacey Jones, Takako I Erdin, Serkan Williamson, Kathleen A Rainger, Joe Stortchevoi, Alexei Samocha, Kaitlin Currall, Benjamin B Dunican, Donncha S Collins, Ryan L Willer, Jason R Lek, Angela Lek, Monkol Nassan, Malik Pereira, Shahrin Kammin, Tammy Lucente, Diane Silva, Alexandra Seabra, Catarina M Chiang, Colby An, Yu Ansari, Morad Rainger, Jacqueline K Joss, Shelagh Smith, Jill Clayton Lippincott, Margaret F Singh, Sylvia S Patel, Nirav Jing, Jenny W Law, Jennifer R Ferraro, Nalton Verloes, Alain Rauch, Anita Steindl, Katharina Zweier, Markus Scheer, Ianina Sato, Daisuke Okamoto, Nobuhiko Jacobsen, Christina Tryggestad, Jeanie Chernausek, Steven Schimmenti, Lisa A Brasseur, Benjamin Cesaretti, Claudia García-Ortiz, Jose E Buitrago, Tatiana Pineda Silva, Orlando Perez Hoffman, Jodi D Mühlbauer, Wolfgang Ruprecht, Klaus W Loeys, Bart L Shino, Masato Kaindl, Angela M Cho, Chie-Hee Morton, Cynthia C Meehan, Richard R van Heyningen, Veronica Liao, Eric C Balasubramanian, Ravikumar Hall, Janet E Seminara, Stephanie B Macarthur, Daniel Moore, Steven A Yoshiura, Koh-Ichiro Gusella, James F Marsh, Joseph A Graham, John M Lin, Angela E Katsanis, Nicholas Jones, Peter L Crowley, William F Davis, Erica E FitzPatrick, David R Talkowski, Michael E Producer: 20170905 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [electronic resource] by Shaw, Natalie D Brand, Harrison Kupchinsky, Zachary A Bengani, Hemant Plummer, Lacey Jones, Takako I Erdin, Serkan Williamson, Kathleen A Rainger, Joe Stortchevoi, Alexei Samocha, Kaitlin Currall, Benjamin B Dunican, Donncha S Collins, Ryan L Willer, Jason R Lek, Angela Lek, Monkol Nassan, Malik Pereira, Shahrin Kammin, Tammy Lucente, Diane Silva, Alexandra Seabra, Catarina M Chiang, Colby An, Yu Ansari, Morad Rainger, Jacqueline K Joss, Shelagh Smith, Jill Clayton Lippincott, Margaret F Singh, Sylvia S Patel, Nirav Jing, Jenny W Law, Jennifer R Ferraro, Nalton Verloes, Alain Rauch, Anita Steindl, Katharina Zweier, Markus Scheer, Ianina Sato, Daisuke Okamoto, Nobuhiko Jacobsen, Christina Tryggestad, Jeanie Chernausek, Steven Schimmenti, Lisa A Brasseur, Benjamin Cesaretti, Claudia García-Ortiz, Jose E Buitrago, Tatiana Pineda Silva, Orlando Perez Hoffman, Jodi D Mühlbauer, Wolfgang Ruprecht, Klaus W Loeys, Bart L Shino, Masato Kaindl, Angela M Cho, Chie-Hee Morton, Cynthia C Meehan, Richard R van Heyningen, Veronica Liao, Eric C Balasubramanian, Ravikumar Hall, Janet E Seminara, Stephanie B Macarthur, Daniel Moore, Steven A Yoshiura, Koh-Ichiro Gusella, James F Marsh, Joseph A Graham, John M Lin, Angela E Katsanis, Nicholas Jones, Peter L Crowley, William F Davis, Erica E FitzPatrick, David R Talkowski, Michael E Publication details: Nature genetics 05 2017 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)