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	181.	Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness. [electronic resource] by Vore, Abram P Chang, Eugene H Hoppe, Jane E Butler, Merlin G Forrester, Shawnia Schneider, Michael C Smith, Luke L H Burke, Daniel W Campbell, Colleen A Smith, Richard J H Producer: 20060110 In: Archives of otolaryngology--head & neck surgery vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study. [electronic resource] by Butler, Merlin G Hartin, Samantha N Hossain, Waheeda A Manzardo, Ann M Kimonis, Virginia Dykens, Elisabeth Gold, June Anne Kim, Soo-Jeong Weisensel, Nicolette Tamura, Roy Miller, Jennifer L Driscoll, Daniel J Producer: 20200514 In: Journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Loxapine add-on for adolescents and adults with autism spectrum disorders and irritability. [electronic resource] by Hellings, Jessica A Reed, Gregory Cain, Sharon E Zhou, Xinghua Barth, Francis X Aman, Michael G Palaguachi, Gladys I Mikhnev, Dmytro Teng, Rujia Andridge, Rebecca Logan, Marilyn Butler, Merlin G Han, Joan C Producer: 20160104 In: Journal of child and adolescent psychopharmacology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years. [electronic resource] by Brothman, Arthur R Schneider, Nancy R Saikevych, Irene Cooley, Linda D Butler, Merlin G Patil, Shivanand Mascarello, James T Rao, Kathleen W Dewald, Gordon W Park, Jonathan P Persons, Diane L Wolff, Daynna J Vance, Gail H Producer: 20060727 In: Archives of pathology & laboratory medicine vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	185.	A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis. [electronic resource] by Zieba, Jennifer Zhang, Wenjuan Chong, Jessica X Forlenza, Kimberly N Martin, Jorge H Heard, Kelly Grange, Dorothy K Butler, Merlin G Kleefstra, Tjitske Lachman, Ralph S Nickerson, Deborah Regnier, Michael Cohn, Daniel H Bamshad, Michael Krakow, Deborah Producer: 20181024 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology. [electronic resource] by Gold, June-Anne Ruth, Chelsey Osann, Kathryn Flodman, Pamela McManus, Barbara Lee, Hye-Seung Donkervoort, Sandra Khare, Manaswitha Roof, Elizabeth Dykens, Elizabeth Miller, Jennifer L Driscoll, Daniel J Butler, Merlin G Heinemann, Janalee Cassidy, Suzanne Kimonis, Virginia E Producer: 20141016 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. [electronic resource] by Radhakrishna, Uppala Nath, Swapan K McElreavey, Ken Ratnamala, Uppala Sun, Celi Maiti, Amit K Gagnebin, Maryline Béna, Frédérique Newkirk, Heather L Sharp, Andrew J Everman, David B Murray, Jeffrey C Schwartz, Charles E Antonarakis, Stylianos E Butler, Merlin G Producer: 20120810 In: Journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. [electronic resource] by Burnside, Rachel D Pasion, Romela Mikhail, Fady M Carroll, Andrew J Robin, Nathaniel H Youngs, Erin L Gadi, Inder K Keitges, Elizabeth Jaswaney, Vikram L Papenhausen, Peter R Potluri, Venkateswara R Risheg, Hiba Rush, Brooke Smith, Janice L Schwartz, Stuart Tepperberg, James H Butler, Merlin G Producer: 20111114 In: Human genetics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients. [electronic resource] by Conway, Robert L Pressman, Barry D Dobyns, William B Danielpour, Moise Lee, John Sanchez-Lara, Pedro A Butler, Merlin G Zackai, Elaine Campbell, Lindsey Saitta, Sulagna C Clericuzio, Carol L Milunsky, Jeff M Hoyme, H Eugene Shieh, Joseph Moeschler, John B Crandall, Barbara Lauzon, Julie L Viskochil, David H Harding, Brian Graham, John M Producer: 20080102 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	190.	Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome. [electronic resource] by Burnett, Lisa C LeDuc, Charles A Sulsona, Carlos R Paull, Daniel Rausch, Richard Eddiry, Sanaa Carli, Jayne F Martin Morabito, Michael V Skowronski, Alicja A Hubner, Gabriela Zimmer, Matthew Wang, Liheng Day, Robert Levy, Brynn Fennoy, Ilene Dubern, Beatrice Poitou, Christine Clement, Karine Butler, Merlin G Rosenbaum, Michael Salles, Jean Pierre Tauber, Maithe Driscoll, Daniel J Egli, Dieter Leibel, Rudolph L Producer: 20170906 In: The Journal of clinical investigation vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	Effects of MetAP2 inhibition on hyperphagia and body weight in Prader-Willi syndrome: A randomized, double-blind, placebo-controlled trial. [electronic resource] by McCandless, Shawn E Yanovski, Jack A Miller, Jennifer Fu, Cary Bird, Lynne M Salehi, Parisa Chan, Christine L Stafford, Diane Abuzzahab, M Jennifer Viskochil, David Barlow, Sarah E Angulo, Moris Myers, Susan E Whitman, Barbara Y Styne, Dennis Roof, Elizabeth Dykens, Elisabeth M Scheimann, Ann O Malloy, Jaret Zhuang, Dongliang Taylor, Kristin Hughes, Thomas E Kim, Dennis D Butler, Merlin G Producer: 20180720 In: Diabetes, obesity & metabolism vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Diphenylbutylpiperidine Antipsychotic Drugs Inhibit Prolactin Receptor Signaling to Reduce Growth of Pancreatic Ductal Adenocarcinoma in Mice. [electronic resource] by Dandawate, Prasad Kaushik, Gaurav Ghosh, Chandrayee Standing, David Ali Sayed, Afreen Asif Choudhury, Sonali Subramaniam, Dharmalingam Manzardo, Ann Banerjee, Tuhina Santra, Santimukul Ramamoorthy, Prabhu Butler, Merlin Padhye, Subhash B Baranda, Joaquina Kasi, Anup Sun, Weijing Tawfik, Ossama Coppola, Domenico Malafa, Mokenge Umar, Shahid Soares, Michael J Saha, Subhrajit Weir, Scott J Dhar, Animesh Jensen, Roy A Thomas, Sufi Mary Anant, Shrikant Producer: 20200710 In: Gastroenterology vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia. [electronic resource] by Heymsfield, Steven B Avena, Nicole M Baier, Leslie Brantley, Phillip Bray, George A Burnett, Lisa C Butler, Merlin G Driscoll, Daniel J Egli, Dieter Elmquist, Joel Forster, Janice L Goldstone, Anthony P Gourash, Linda M Greenway, Frank L Han, Joan C Kane, James G Leibel, Rudolph L Loos, Ruth J F Scheimann, Ann O Roth, Christian L Seeley, Randy J Sheffield, Val Tauber, Maïthé Vaisse, Christian Wang, Liheng Waterland, Robert A Wevrick, Rachel Yanovski, Jack A Zinn, Andrew R Producer: 20140901 In: Obesity (Silver Spring, Md.) vol. 22 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	194.	Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. [electronic resource] by Burrage, Lindsay C Reynolds, John J Baratang, Nissan Vida Phillips, Jennifer B Wegner, Jeremy McFarquhar, Ashley Higgs, Martin R Christiansen, Audrey E Lanza, Denise G Seavitt, John R Jain, Mahim Li, Xiaohui Parry, David A Raman, Vandana Chitayat, David Chinn, Ivan K Bertuch, Alison A Karaviti, Lefkothea Schlesinger, Alan E Earl, Dawn Bamshad, Michael Savarirayan, Ravi Doddapaneni, Harsha Muzny, Donna Jhangiani, Shalini N Eng, Christine M Gibbs, Richard A Bi, Weimin Emrick, Lisa Rosenfeld, Jill A Postlethwait, John Westerfield, Monte Dickinson, Mary E Beaudet, Arthur L Ranza, Emmanuelle Huber, Celine Cormier-Daire, Valérie Shen, Wei Mao, Rong Heaney, Jason D Orange, Jordan S Bertola, Débora Yamamoto, Guilherme L Baratela, Wagner A R Butler, Merlin G Ali, Asim Adeli, Mehdi Cohn, Daniel H Krakow, Deborah Jackson, Andrew P Lees, Melissa Offiah, Amaka C Carlston, Colleen M Carey, John C Stewart, Grant S Bacino, Carlos A Campeau, Philippe M Lee, Brendan Producer: 20191218 In: American journal of human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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