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	461.	How and where are nonsense mRNAs degraded in mammalian cells? [electronic resource] by Mühlemann, Oliver Lykke-Andersen, Jens Producer: 20101103 In: RNA biology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	462.	X-linked myotubular myopathy in a family with two infant siblings: a case with MTM1 mutation. [electronic resource] by Jeon, Ji Hyun Namgung, Ran Park, Min Soo Park, Kook In Lee, Chul Lee, Jin Sung Kim, Se Hoon Producer: 20110908 In: Yonsei medical journal vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	463.	Craniosynostosis: a previously unreported association with CHST3-related skeletal dysplasia (autosomal recessive Larsen syndrome). [electronic resource] by Searle, Claire Jewell, Rosalyn Kraft, Jeannette Stoebe, Petra Chumas, Paul Titheradge, Hannah Kraus, Alison Gencik, Martin Hobson, Emma Producer: 20140721 In: Clinical dysmorphology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	464.	A novel nonsense mutation in the tyrosinase gene is related to the albinism in a capuchin monkey (Sapajus apella). [electronic resource] by Galante Rocha de Vasconcelos, Felipe Tadeu Hauzman, Einat Dutra Henriques, Leonardo Kilpp Goulart, Paulo Roney de Faria Galvão, Olavo Sano, Ronaldo Yuiti da Silva Souza, Givago Lynch Alfaro, Jessica de Lima Silveira, Luis Carlos Fix Ventura, Dora Oliveira Bonci, Daniela Maria Producer: 20171006 In: BMC genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	465.	A nonsense mutation in the FGF5 gene is associated with the long-haired phenotype in domestic guinea pigs (Cavia porcellus). [electronic resource] by Yu, Feng Liu, Zhengxi Jiao, Shuyu Zhang, Xiaoying Bai, Chunyan Zhang, Jiabao Yan, Shouqing Producer: 20181101 In: Animal genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	466.	Multiple miscarriages in two sisters of Thai origin with the rare P [electronic resource] by Ricci Hagman, J Hult, A K Westman, J S Hosseini-Maaf, B Jongruamklang, P Saipin, J Bejrachandra, S Olsson, M L Producer: 20191225 In: Transfusion medicine (Oxford, England) vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	467.	A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report. [electronic resource] by Ma, Di Shen, Shanshan Gao, Hui Guo, Hui Lin, Yumei Hu, Yuhua Zhang, Ruanzhang Wang, Shayan Producer: 20190415 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	468.	Biallelic TOR1A mutations cause severe arthrogryposis: A case requiring reverse phenotyping. [electronic resource] by Isik, Esra Aykut, Ayca Atik, Tahir Cogulu, Ozgur Ozkinay, Ferda Producer: 20200120 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	469.	Detection of homozygous genotypes for a putatively lethal recessive mutation in the porcine argininosuccinate synthase 1 (ASS1) gene. [electronic resource] by Mármol-Sánchez, E Luigi-Sierra, M G Quintanilla, R Amills, M Producer: 20200213 In: Animal genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	470.	[Of mice and men: pathogenesis and treatment of obesity in genetic perspective]. [electronic resource] by Pijl, H Meinders, A E Producer: 19960116 In: Nederlands tijdschrift voor geneeskunde vol. 139 Availability: No items available. Save to lists Add to cart (remove)
	471.	A novel nonsense mutation (515del4) in muscle carnitine palmitoyltransferase II deficiency. [electronic resource] by Deschauer, Marcus Wieser, Thomas Schröder, Rolf Zierz, Stephan Producer: 20020521 In: Molecular genetics and metabolism vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	472.	Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia. [electronic resource] by Ono, Hiroaki Sakura, Nobuo Yamashita, Katsuko Yuasa, Isao Ohno, Kousaku Producer: 20031121 In: Brain & development vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	473.	Nonsense-mediated decay breaks the circle? [electronic resource] by Graham, Sheila V Producer: 20030922 In: The Biochemical journal vol. 373 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	474.	Gene symbol: SLC3A1. Disease: cystinuria. [electronic resource] by Nunes, V Font-Llitjós, M Jiménez-Vidal, M Bisceglia, L Di Perna, M de Sanctis, L Rousad, F Zelante, L Palacín, M Producer: 20050412 In: Human genetics vol. 116 Availability: No items available. Save to lists Add to cart (remove)
	475.	Gene symbol: SLC3A1. Disease: cystinuria. [electronic resource] by Nunes, V Font-Llitjós, M Jiménez-Vidal, M Bisceglia, L Di Perna, M de Sanctis, L Rousaud, F Zelante, L Palacín, M Producer: 20050412 In: Human genetics vol. 116 Availability: No items available. Save to lists Add to cart (remove)
	476.	The distribution of constitutional and somatic mutations in the neurofibromatosis 2 gene. [electronic resource] by Baser, Michael E Producer: 20061226 In: Human mutation vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	477.	Gene symbol: mc4r. Disease: obesity. [electronic resource] by Jia, W P Producer: 20060321 In: Human genetics vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	478.	Severe hyperbilirubinaemia in a Chinese girl with type I Crigler-Najjar syndrome: first case ever reported in Mainland China. [electronic resource] by Nong, Shao-Han Xie, Yan-Ming Chan, Koon-Wing Cheung, Pik-To Producer: 20051025 In: Journal of paediatrics and child health vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	479.	Genome-wide identification of alternative splice forms down-regulated by nonsense-mediated mRNA decay in Drosophila. [electronic resource] by Hansen, Kasper Daniel Lareau, Liana F Blanchette, Marco Green, Richard E Meng, Qi Rehwinkel, Jan Gallusser, Fabian L Izaurralde, Elisa Rio, Donald C Dudoit, Sandrine Brenner, Steven E Producer: 20090909 In: PLoS genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	480.	Novel human pathological mutations. Gene symbol: SPRED1. Disease: Legius syndrome. [electronic resource] by Jim, Hoi Ping Upadhyaya, Meena Producer: 20100217 In: Human genetics vol. 127 Availability: No items available. Save to lists Add to cart (remove)

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