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	3221.	Whole exome sequencing analysis of urine trans-renal tumour DNA in metastatic colorectal cancer patients. [electronic resource] by Crisafulli, Giovanni Mussolin, Benedetta Cassingena, Andrea Montone, Monica Bartolini, Alice Barault, Ludovic Martinetti, Antonia Morano, Federica Pietrantonio, Filippo Sartore-Bianchi, Andrea Siena, Salvatore Di Nicolantonio, Federica Marsoni, Silvia Bardelli, Alberto Siravegna, Giulia Producer: 20200615 In: ESMO open vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3222.	Endothelial Pannexin 1 Channels Control Inflammation by Regulating Intracellular Calcium. [electronic resource] by Yang, Yang Delalio, Leon J Best, Angela K Macal, Edgar Milstein, Jenna Donnelly, Iona Miller, Ashley M McBride, Martin Shu, Xiaohong Koval, Michael Isakson, Brant E Johnstone, Scott R Producer: 20210308 In: Journal of immunology (Baltimore, Md. : 1950) vol. 204 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3223.	Immunohistochemical and genetic characteristics of lung cancer mimicking organizing pneumonia. [electronic resource] by Ichikawa, Tomohiro Saruwatari, Koichi Mimaki, Sachiyo Sugano, Masato Aokage, Keiju Kojima, Motohiro Hishida, Tomoyuki Fujii, Satoshi Yoshida, Junji Kuwata, Takeshi Ochiai, Atsushi Suzuki, Kenji Tsuboi, Masahiro Goto, Koichi Tsuchihara, Katsuya Ishii, Genichiro Producer: 20180625 In: Lung cancer (Amsterdam, Netherlands) vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3224.	The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome. [electronic resource] by Vidal, Silvia Brandi, Núria Pacheco, Paola Gerotina, Edgar Blasco, Laura Trotta, Jean-Rémi Derdak, Sophia Del Mar O'Callaghan, Maria Garcia-Cazorla, Àngels Pineda, Mercè Armstrong, Judith Producer: 20190716 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3225.	High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder. [electronic resource] by Tombácz, Dóra Maróti, Zoltán Kalmár, Tibor Csabai, Zsolt Balázs, Zsolt Takahashi, Shinichi Palkovits, Miklós Snyder, Michael Boldogkői, Zsolt Producer: 20190218 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3226.	Whole-exome sequencing of cell-free DNA and circulating tumor cells in multiple myeloma. [electronic resource] by Manier, S Park, J Capelletti, M Bustoros, M Freeman, S S Ha, G Rhoades, J Liu, C J Huynh, D Reed, S C Gydush, G Salem, K Z Rotem, D Freymond, C Yosef, A Perilla-Glen, A Garderet, L Van Allen, E M Kumar, S Love, J C Getz, G Adalsteinsson, V A Ghobrial, I M Producer: 20181211 In: Nature communications vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3227.	Differences between BCL2-break positive and negative follicular lymphoma unraveled by whole-exome sequencing. [electronic resource] by Zamò, A Pischimarov, J Schlesner, M Rosenstiel, P Bomben, R Horn, H Grieb, T Nedeva, T López, C Haake, A Richter, J Trümper, L Lawerenz, C Klapper, W Möller, P Hummel, M Lenze, D Szczepanowski, M Flossbach, L Schreder, M Gattei, V Ott, G Siebert, R Rosenwald, A Leich, E Producer: 20190208 In: Leukemia vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3228.	Alzheimer disease associated variants in SORL1 accelerate dementia development in Parkinson disease. [electronic resource] by Maple-Grødem, Jodi Chung, Janete Lunde, Kristin Aaser Tzoulis, Charalampos Tysnes, Ole-Bjørn Pedersen, Kenn Freddy Alves, Guido Producer: 20190225 In: Neuroscience letters vol. 674 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3229.	A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families. [electronic resource] by Hartley, Jessica N Simard, Louise R Ly, Valentina Del Bigio, Marc R Frosk, Patrick Producer: 20200206 In: American journal of medical genetics. Part A vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3230.	Revisiting aneuploidy profile of surgically retrieved spermatozoa by whole exome sequencing molecular karyotype. [electronic resource] by Cheung, Stephanie Schlegel, Peter N Rosenwaks, Zev Palermo, Gianpiero D Producer: 20190930 In: PloS one vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3231.	De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report. [electronic resource] by Mavros, Chrystal F Brownstein, Catherine A Thyagrajan, Roshni Genetti, Casie A Tembulkar, Sahil Graber, Kelsey Murphy, Quinn Cabral, Kristin VanNoy, Grace E Bainbridge, Matthew Shi, Jiahai Agrawal, Pankaj B Beggs, Alan H D'Angelo, Eugene Gonzalez-Heydrich, Joseph Producer: 20190522 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3232.	Depletion of the Transcriptional Coactivator Amplified in Breast Cancer 1 (AIB1) Uncovers Functionally Distinct Subpopulations in Triple-Negative Breast Cancer. [electronic resource] by Saenz, F R Ory, V Schmidt, M O Kallakury, B V Mueller, S C Furth, P A Wellstein, A Riegel, A T Producer: 20200421 In: Neoplasia (New York, N.Y.) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3233.	AKT1 internal tandem duplications and point mutations are the genetic hallmarks of sclerosing pneumocytoma. [electronic resource] by Yeh, Yi-Chen Ho, Hsiang-Ling Wu, Yu-Chung Pan, Chin-Chen Wang, Yu-Chao Chou, Teh-Ying Producer: 20210125 In: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3234.	Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans. [electronic resource] by Cox, Timothy C Lidral, Andrew C McCoy, Jason C Liu, Huan Cox, Liza L Zhu, Ying Anderson, Ryan D Moreno Uribe, Lina M Anand, Deepti Deng, Mei Richter, Chika T Nidey, Nichole L Standley, Jennifer M Blue, Elizabeth E Chong, Jessica X Smith, Joshua D Kirk, Edwin P Venselaar, Hanka Krahn, Katy N van Bokhoven, Hans Zhou, Huiqing Cornell, Robert A Glass, Ian A Bamshad, Michael J Nickerson, Deborah A Murray, Jeffrey C Lachke, Salil A Thompson, Thomas B Buckley, Michael F Roscioli, Tony Producer: 20200309 In: Human mutation vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3235.	Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran. [electronic resource] by Shahbazi, Zahra Yazdani, Reza Shahkarami, Sepideh Shahbazi, Shirin Hamid, Mohammad Sadeghi-Shabestari, Mahnaz Momen, Tooba Aleyasin, Soheila Esmaeilzadeh, Hossein Darougar, Sepideh Delavari, Sama Mahdaviani, Seyed Alireza Ahanchian, Hamid Behmanesh, Fatemeh Kiaee, Fatemeh Chavoshzade, Zahra Shariat, Mansoureh Keramatipour, Mohammad Rezaei, Nima Abolhassani, Hassan Parvaneh, Nima Mahdian, Reza Aghamohammadi, Asghar Producer: 20200527 In: Immunology letters vol. 216 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3236.	Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing. [electronic resource] by Musolf, Anthony M Ho, Winson S C Long, Kyle A Zhuang, Zhengping Argersinger, Davis P Sun, Haiming Moiz, Bilal A Simpson, Claire L Mendelevich, Elena G Bogdanov, Enver I Bailey-Wilson, Joan E Heiss, John D Producer: 20200616 In: European journal of human genetics : EJHG vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3237.	Carrier screening for single gene disorders. [electronic resource] by Rose, Nancy C Wick, Myra Producer: 20181211 In: Seminars in fetal & neonatal medicine vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3238.	TCR Repertoire Intratumor Heterogeneity in Localized Lung Adenocarcinomas: An Association with Predicted Neoantigen Heterogeneity and Postsurgical Recurrence. [electronic resource] by Reuben, Alexandre Gittelman, Rachel Gao, Jianjun Zhang, Jiexin Yusko, Erik C Wu, Chang-Jiun Emerson, Ryan Zhang, Jianhua Tipton, Christopher Li, Jun Quek, Kelly Gopalakrishnan, Vancheswaran Chen, Runzhe Vence, Luis M Cascone, Tina Vignali, Marissa Fujimoto, Junya Rodriguez-Canales, Jaime Parra, Edwin R Little, Latasha D Gumbs, Curtis Forget, Marie-Andrée Federico, Lorenzo Haymaker, Cara Behrens, Carmen Benzeno, Sharon Bernatchez, Chantale Sepesi, Boris Gibbons, Don L Wargo, Jennifer A William, William N Swisher, Stephen Heymach, John V Robins, Harlan Lee, J Jack Sharma, Padmanee Allison, James P Futreal, P Andrew Wistuba, Ignacio I Zhang, Jianjun Producer: 20180521 In: Cancer discovery vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3239.	FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1. [electronic resource] by Khan, Shahid Y Vasanth, Shivakumar Kabir, Firoz Gottsch, John D Khan, Arif O Chaerkady, Raghothama Lee, Mei-Chong W Leitch, Carmen C Ma, Zhiwei Laux, Julie Villasmil, Rafael Khan, Shaheen N Riazuddin, Sheikh Akram, Javed Cole, Robert N Talbot, C Conover Pourmand, Nader Zaghloul, Norann A Hejtmancik, J Fielding Riazuddin, S Amer Producer: 20180626 In: Nature communications vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3240.	Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples. [electronic resource] by Wang, Jingwen Skoog, Tiina Einarsdottir, Elisabet Kaartokallio, Tea Laivuori, Hannele Grauers, Anna Gerdhem, Paul Hytönen, Marjo Lohi, Hannes Kere, Juha Jiao, Hong Producer: 20180530 In: Scientific reports vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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