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	41.	Degree of external genital malformation at birth in children with a disorder of sex development and subsequent caregiver distress. [electronic resource] by Wolfe-Christensen, Cortney Fedele, David A Kirk, Katherine Phillips, Timothy M Mazur, Tom Mullins, Larry L Chernausek, Steven D Lakshmanan, Yegappan Wisniewski, Amy B Producer: 20121231 In: The Journal of urology vol. 188 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	An Evidence-Based Model of Multidisciplinary Care for Patients and Families Affected by Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. [electronic resource] by Schaeffer, Traci L Tryggestad, Jeanie B Mallappa, Ashwini Hanna, Adam E Krishnan, Sowmya Chernausek, Steven D Chalmers, Laura J Reiner, William G Kropp, Brad P Wisniewski, Amy B Producer: 20110714 In: International journal of pediatric endocrinology vol. 2010 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Beta cell function and insulin sensitivity in obese youth with maturity onset diabetes of youth mutations vs type 2 diabetes in TODAY: Longitudinal observations and glycemic failure. [electronic resource] by Arslanian, Silva El Ghormli, Laure Haymond, Morey H Chan, Christine L Chernausek, Steven D Gandica, Rachelle G Gubitosi-Klug, Rose Levitsky, Lynne L Siska, Maggie Willi, Steven M Producer: 20210615 In: Pediatric diabetes vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	A model of delivering multi-disciplinary care to people with 46 XY DSD. [electronic resource] by Palmer, Blake W Wisniewski, Amy B Schaeffer, Traci L Mallappa, Ashwini Tryggestad, Jeanie B Krishnan, Sowmya Chalmers, Laura J Copeland, Kenneth Chernausek, Steven D Reiner, William G Kropp, Bradley P Producer: 20120628 In: Journal of pediatric urology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation. [electronic resource] by Abuzzahab, M Jennifer Schneider, Anke Goddard, Audrey Grigorescu, Florin Lautier, Corinne Keller, Eberhard Kiess, Wieland Klammt, Jürgen Kratzsch, Jürgen Osgood, Doreen Pfäffle, Roland Raile, Klemens Seidel, Berthold Smith, Robert J Chernausek, Steven D Producer: 20031211 In: The New England journal of medicine vol. 349 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Proceedings from the Turner Resource Network symposium: the crossroads of health care research and health care delivery. [electronic resource] by Backeljauw, Philippe F Bondy, Carolyn Chernausek, Steven D Cernich, Joseph T Cole, David A Fasciano, Laura P Foodim, Joan Hawley, Scott Hong, David S Knickmeyer, Rebecca C Kruszka, Paul Lin, Angela E Lippe, Barbara M Lorigan, Gary A Maslen, Cheryl L Mauras, Nelly Page, David C Pemberton, Victoria L Prakash, Siddharth K Quigley, Charmian A Ranallo, Kelly C Reiss, Allan L Sandberg, David E Scurlock, Cindy Silberbach, Michael Producer: 20160519 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	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)
	48.	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)