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	1221.	Identification of novel splice variants of the human CD44 gene. [electronic resource] by Vela, Elena Roca, Xavier Isamat, Marcos Producer: 20060524 In: Biochemical and biophysical research communications vol. 343 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1222.	Aberrant termination triggers nonsense-mediated mRNA decay. [electronic resource] by Amrani, N Dong, S He, F Ganesan, R Ghosh, S Kervestin, S Li, C Mangus, D A Spatrick, P Jacobson, A Producer: 20060327 In: Biochemical Society transactions vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1223.	Psi-Phi: exploring the outer limits of bacterial pseudogenes. [electronic resource] by Lerat, Emmanuelle Ochman, Howard Producer: 20050119 In: Genome research vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1224.	Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations. [electronic resource] by Castaman, G Giacomelli, S H Duga, S Rodeghiero, F Producer: 20081231 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1225.	Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia. [electronic resource] by Cefalù, Angelo B Noto, Davide Arpi, Maria Luisa Yin, Fen Spina, Rossella Hilden, Hannele Barbagallo, Carlo M Carroccio, Antonio Tarugi, Patrizia Squatrito, Sebastiano Vigneri, Riccardo Taskinen, Marja-Riitta Péterfy, Miklós Averna, Maurizio R Producer: 20100107 In: The Journal of clinical endocrinology and metabolism vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1226.	Chemical biology: ignore the nonsense. [electronic resource] by Schmitz, Anton Famulok, Michael Producer: 20070522 In: Nature vol. 447 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1227.	Recurrence of the 'deep-intronic' FGG IVS6-320A>T mutation causing quantitative fibrinogen deficiency in the Italian population of Veneto. [electronic resource] by Platè, Manuela Duga, Stefano Castaman, Giancarlo Rodeghiero, Francesco Asselta, Rosanna Producer: 20090824 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1228.	Phenotypic variation in FAM83H-associated amelogenesis imperfecta. [electronic resource] by Wright, J T Frazier-Bowers, S Simmons, D Alexander, K Crawford, P Han, S T Hart, P S Hart, T C Producer: 20090529 In: Journal of dental research vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1229.	Posttranscriptional gene regulation by spatial rearrangement of the 3' untranslated region. [electronic resource] by Eberle, Andrea B Stalder, Lukas Mathys, Hansruedi Orozco, Rodolfo Zamudio Mühlemann, Oliver 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)
	1230.	Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome. [electronic resource] by Moheb, Lia Abbasi Tzschach, Andreas Garshasbi, Masoud Kahrizi, Kimia Darvish, Hossein Heshmati, Yaser Kordi, Alireza Najmabadi, Hossein Ropers, Hans Hilger Kuss, Andreas Walter Producer: 20080422 In: European journal of human genetics : EJHG vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1231.	Transcripts from a novel BMPR2 termination mutation escape nonsense mediated decay by downstream translation re-initiation: implications for treating pulmonary hypertension. [electronic resource] by Hamid, R Hedges, L K Austin, E Phillips, J A Loyd, J E Cogan, J D Producer: 20100706 In: Clinical genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1232.	Nonsense-mediated RNA decay regulation by cellular stress: implications for tumorigenesis. [electronic resource] by Gardner, Lawrence B Producer: 20100712 In: Molecular cancer research : MCR vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1233.	mRNA stability and control of cell proliferation. [electronic resource] by Mazzoni, Cristina Falcone, Claudio Producer: 20120117 In: Biochemical Society transactions vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1234.	FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia. [electronic resource] by Naz, G Pasternack, S M Perrin, C Mattheisen, M Refke, M Khan, S Gul, A Simons, M Ahmad, W Betz, R C Producer: 20120709 In: The British journal of dermatology vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1235.	A novel nonsense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a Pakistani family. [electronic resource] by Wasif, Naveed Ahmad, Wasim Producer: 20130807 In: Pediatric dermatology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1236.	Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay. [electronic resource] by Lynch, Sally Ann Nguyen, Lam Son Ng, Li Yen Waldron, Mary McDonald, Denise Gecz, Jozef Producer: 20121126 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1237.	T- and B-cell defects in a novel purine nucleoside phosphorylase mutation. [electronic resource] by Somech, Raz Lev, Atar Simon, Amos J Hanna, Suhair Etzioni, Amos Producer: 20121017 In: The Journal of allergy and clinical immunology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1238.	Limitations of the rhesus macaque draft genome assembly and annotation. [electronic resource] by Zhang, Xiongfei Goodsell, Joel Norgren, Robert B Producer: 20121219 In: BMC genomics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1239.	Pediatric case report: clinical profile of a patient with PCWH with p.Q377X nonsense mutation in the SOX10 gene. [electronic resource] by Oshimo, Tomoko Fukai, Kazuyoshi Abe, Yuko Hozumi, Yutaka Yokoi, Toshiaki Tanaka, Akemi Yamanishi, Kiyofumi Ishii, Masamitsu Suzuki, Tamio Producer: 20140109 In: The Journal of dermatology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1240.	Exome sequencing establishes diagnosis of Alström syndrome in an infant presenting with non-syndromic dilated cardiomyopathy. [electronic resource] by Long, Pamela A Evans, Jared M Olson, Timothy M Producer: 20151214 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)

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