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	3581.	An expanded eukaryotic genetic code. [electronic resource] by Chin, Jason W Cropp, T Ashton Anderson, J Christopher Mukherji, Mridul Zhang, Zhiwen Schultz, Peter G Producer: 20030908 In: Science (New York, N.Y.) vol. 301 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3582.	Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort. [electronic resource] by Dent, K M Dunn, D M von Niederhausern, A C Aoyagi, A T Kerr, L Bromberg, M B Hart, K J Tuohy, T White, S den Dunnen, J T Weiss, R B Flanigan, K M Producer: 20050509 In: American journal of medical genetics. Part A vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3583.	Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis. [electronic resource] by Chen, Chih-Ping Su, Yi-Ning Hung, Chia-Cheng Shih, Jin-Chung Wang, Wayseen Producer: 20060823 In: Journal of the Formosan Medical Association = Taiwan yi zhi vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3584.	Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14. [electronic resource] by Lugassy, Jennie Itin, Peter Ishida-Yamamoto, Akemi Holland, Kristen Huson, Susan Geiger, Dan Hennies, Hans Christian Indelman, Margarita Bercovich, Dani Uitto, Jouni Bergman, Reuven McGrath, John A Richard, Gabriele Sprecher, Eli Producer: 20061031 In: American journal of human genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3585.	The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay. [electronic resource] by Harries, L W Bingham, Coralie Bellanne-Chantelot, Christine Hattersley, A T Ellard, Sian Producer: 20060330 In: Human genetics vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3586.	NMD microarray analysis for rapid genome-wide screen of mutated genes in cancer. [electronic resource] by Wolf, Maija Edgren, Henrik Muggerud, Aslaug Kilpinen, Sami Huusko, Pia Sørlie, Therese Mousses, Spyro Kallioniemi, Olli Producer: 20051213 In: Cellular oncology : the official journal of the International Society for Cellular Oncology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3587.	Detection of germline mutations in argentine retinoblastoma patients: low and full penetrance retinoblastoma caused by the same germline truncating mutation. [electronic resource] by Dalamón, Viviana Surace, Ezequiel Giliberto, Florencia Ferreiro, Verónica Fernandez, Cecilia Szijan, Irene Producer: 20041028 In: Journal of biochemistry and molecular biology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3588.	Defective assembly and trafficking of mutant HERG channels with C-terminal truncations in long QT syndrome. [electronic resource] by Gong, Qiuming Keeney, David R Robinson, Jeffrey C Zhou, Zhengfeng Producer: 20050419 In: Journal of molecular and cellular cardiology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3589.	Arg120stop nonsense mutation in the RP2 gene: mutational hotspot and germ line mosaicism? [electronic resource] by Vorster, A A Rebello, M T Coutts, N Ehrenreich, L Gama, A D Roberts, L J Goliath, R Ramesar, R Greenberg, L J Producer: 20040831 In: Clinical genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3590.	A particular phenotype in a girl with aldosterone synthase deficiency. [electronic resource] by Williams, Tracy A Mulatero, Paolo Bosio, Maurizio Lewicka, Sabina Palermo, Mario Veglio, Franco Armanini, Decio Producer: 20040810 In: The Journal of clinical endocrinology and metabolism vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3591.	Identification of mutations in the myocilin (MYOC) gene in Taiwanese patients with juvenile-onset open-angle glaucoma. [electronic resource] by Yen, Yung-Chang Yang, Jiann-Jou Chou, Ming-Chih Li, Shuan-Yow Producer: 20071023 In: Molecular vision vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	3592.	UPF1, a conserved nonsense-mediated mRNA decay factor, regulates cyst wall protein transcripts in Giardia lamblia. [electronic resource] by Chen, Yi-Hsiu Su, Li-Hsin Huang, Yu-Chang Wang, Yi-Ting Kao, Yu-Yun Sun, Chin-Hung Producer: 20090212 In: PloS one vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3593.	cDNA sequencing improves the detection of P53 missense mutations in colorectal cancer. [electronic resource] by Szybka, Malgorzata Zakrzewska, Magdalena Rieske, Piotr Pasz-Walczak, Grazyna Kulczycka-Wojdala, Dominika Zawlik, Izabela Stawski, Robert Jesionek-Kupnicka, Dorota Liberski, Pawel P Kordek, Radzislaw Producer: 20091211 In: BMC cancer vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3594.	A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction. [electronic resource] by Henderson, Robert H Williamson, Kathleen A Kennedy, Joanna S Webster, Andrew R Holder, Graham E Robson, Anthony G FitzPatrick, David R van Heyningen, Veronica Moore, Anthony T Producer: 20091230 In: Molecular vision vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	3595.	Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypes. [electronic resource] by Fry, Andrew E Ghansa, Anita Small, Kerrin S Palma, Alejandro Auburn, Sarah Diakite, Mahamadou Green, Angela Campino, Susana Teo, Yik Y Clark, Taane G Jeffreys, Anna E Wilson, Jonathan Jallow, Muminatou Sisay-Joof, Fatou Pinder, Margaret Griffiths, Michael J Peshu, Norbert Williams, Thomas N Newton, Charles R Marsh, Kevin Molyneux, Malcolm E Taylor, Terrie E Koram, Kwadwo A Oduro, Abraham R Rogers, William O Rockett, Kirk A Sabeti, Pardis C Kwiatkowski, Dominic P Producer: 20090914 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3596.	A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent Müllerian duct syndrome. [electronic resource] by Wu, Xiufeng Wan, Shengqin Pujar, Shashikant Haskins, Mark E Schlafer, Donald H Lee, Mary M Meyers-Wallen, Vicki N Producer: 20090219 In: Journal of andrology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3597.	Genetic alterations in members of the Wnt pathway in acute leukemia. [electronic resource] by Erbilgin, Yucel Ng, Ozden Hatirnaz Mavi, Nurhan Ozbek, Ugur Sayitoglu, Muge Producer: 20120803 In: Leukemia & lymphoma vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3598.	A competition between stimulators and antagonists of Upf complex recruitment governs human nonsense-mediated mRNA decay. [electronic resource] by Singh, Guramrit Rebbapragada, Indrani Lykke-Andersen, Jens Producer: 20080708 In: PLoS biology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3599.	Sequence analysis of three pigmentation genes in the Newfoundland population of Canis latrans links the Golden Retriever Mc1r variant to white coat color in coyotes. [electronic resource] by Brockerville, Ryan M McGrath, Michael J Pilgrim, Brettney L Marshall, H Dawn Producer: 20131031 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3600.	A common variant in the Von Willebrand factor gene is associated with multiple functional consequences. [electronic resource] by Vaidya, Dhananjay Yanek, Lisa R Herrera-Galeano, J Enrique Mathias, Rasika A Moy, Taryn F Faraday, Nauder Becker, Lewis C Becker, Diane M Producer: 20101228 In: American journal of hematology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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