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	2361.	A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family. [electronic resource] by Anjanappa, Ram M Nayak, Sourav Moily, Nagaraj S Manduva, Vallikiran Nadella, Ravi K Viswanath, Biju Reddy, Yemmiganur C J Jain, Sanjeev Anand, Anuranjan Producer: 20200817 In: Bipolar disorders vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2362.	Homozygous mutations in [electronic resource] by Wang, Wenjing Dong, Jie Chen, Biaobang Du, Jing Kuang, Yanping Sun, Xiaoxi Fu, Jing Li, Bin Mu, Jian Zhang, Zhihua Zhou, Zhou Lin, Zhao Wu, Ling Yan, Zheng Mao, Xiaoyan Li, Qiaoli He, Lin Wang, Lei Sang, Qing Producer: 20210226 In: Journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2363.	Pathway Mutations in Breast Cancer Using Whole-Exome Sequencing. [electronic resource] by Chang, Ya-Sian Chang, Chieh-Min Lin, Chien-Yu Chao, Dy-San Huang, Hsi-Yuan Chang, Jan-Gowth Producer: 20200918 In: Oncology research vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2364.	Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia. [electronic resource] by Verdura, Edgard Fons, Carme Schlüter, Agatha Ruiz, Montserrat Fourcade, Stéphane Casasnovas, Carlos Castellano, Antonio Pujol, Aurora Producer: 20210202 In: Journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2365.	Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism. [electronic resource] by Sjaarda, Calvin P Wood, Shalandra McNaughton, Amy J M Taylor, Sarah Hudson, Melissa L Liu, Xudong Guerin, Andrea Ayub, Muhammad Producer: 20201009 In: Journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2366.	Latency and interval therapy affect the evolution in metastatic colorectal cancer. [electronic resource] by Nikbakht, Hamid Jessa, Selin Sukhai, Mahadeo A Arseneault, Madeleine Zhang, Tong Letourneau, Louis Thomas, Mariam Bourgey, Mathieu Roehrl, Michael H A Eveleigh, Robert Chen, Eric X Krzyzanowska, Monika Moore, Malcolm J Giesler, Amanda Yu, Celeste Bedard, Philippe L Kamel-Reid, Suzanne Majewski, Jacek Siu, Lillian L Riazalhosseini, Yasser Graham, Donna M Producer: 20201119 In: Scientific reports vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2367.	None [electronic resource] by Lyon, Gholson J Marchi, Elaine Ekstein, Joseph Meiner, Vardiella Hirsch, Yoel Scher, Sholem Yang, Edward De Vivo, Darryl C Madrid, Ricardo Li, Quan Wang, Kai Haworth, Andrea Chilton, Ilana Chung, Wendy K Velinov, Milen Producer: 20200821 In: Cold Spring Harbor molecular case studies vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2368.	Disparity between Inter-Patient Molecular Heterogeneity and Repertoires of Target Drugs Used for Different Types of Cancer in Clinical Oncology. [electronic resource] by Zolotovskaia, Marianna A Sorokin, Maxim I Petrov, Ivan V Poddubskaya, Elena V Moiseev, Alexey A Sekacheva, Marina I Borisov, Nicolas M Tkachev, Victor S Garazha, Andrew V Kaprin, Andrey D Shegay, Peter V Giese, Alf Kim, Ella Roumiantsev, Sergey A Buzdin, Anton A Producer: 20201208 In: International journal of molecular sciences vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2369.	Homozygosity for a missense variant in COMP gene associated with severe pseudoachondroplasia. [electronic resource] by Tariq, M Khan, T N Lundin, L Jameel, M Lönnerholm, T Baig, S M Dahl, N Klar, J Producer: 20180806 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2370.	Hemolytic anemia with null PKLR mutations identified using whole exome sequencing and cured by hematopoietic stem cell transplantation combined with splenectomy. [electronic resource] by Kim, M Park, J Lee, J Jang, W Chae, H Choi, H Kim, J Kwon, A Lee, J-W Cho, B Kim, Y Chung, N-G Producer: 20180206 In: Bone marrow transplantation vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2371.	Biallelic variants in WARS2 encoding mitochondrial tryptophanyl-tRNA synthase in six individuals with mitochondrial encephalopathy. [electronic resource] by Wortmann, Saskia B Timal, Sharita Venselaar, Hanka Wintjes, Liesbeth T Kopajtich, Robert Feichtinger, René G Onnekink, Carla Mühlmeister, Mareike Brandt, Ulrich Smeitink, Jan A Veltman, Joris A Sperl, Wolfgang Lefeber, Dirk Pruijn, Ger Stojanovic, Vesna Freisinger, Peter V Spronsen, Francjan Derks, Terry Gj Veenstra-Knol, Hermine E Mayr, Johannes A Rötig, Agnes Tarnopolsky, Mark Prokisch, Holger Rodenburg, Richard J Producer: 20180618 In: Human mutation vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2372.	A unique de novo gain-of-function variant in [electronic resource] by Zech, Michael Lam, Daniel D Weber, Sandrina Berutti, Riccardo Poláková, Kamila Havránková, Petra Fečíková, Anna Strom, Tim M Růžička, Evžen Jech, Robert Winkelmann, Juliane Producer: 20190917 In: Cold Spring Harbor molecular case studies vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2373.	Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course. [electronic resource] by Gil-Varea, Elia Urcelay, Elena Vilariño-Güell, Carles Costa, Carme Midaglia, Luciana Matesanz, Fuencisla Rodríguez-Antigüedad, Alfredo Oksenberg, Jorge Espino-Paisan, Laura Dessa Sadovnick, A Saiz, Albert Villar, Luisa M García-Merino, Juan Antonio Ramió-Torrentà, Lluís Triviño, Juan Carlos Quintana, Ester Robles, René Sánchez-López, Antonio Arroyo, Rafael Alvarez-Cermeño, Jose C Vidal-Jordana, Angela Malhotra, Sunny Fissolo, Nicolas Montalban, Xavier Comabella, Manuel Producer: 20181211 In: Journal of neuroinflammation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2374.	Genetic heterogeneity and mutational signature in Chinese Epstein-Barr virus-positive diffuse large B-cell lymphoma. [electronic resource] by Liu, Fang Wang, Zhe Zhou, Xiaoge Liu, Qing Chen, Gang Xiao, Hualiang Yin, Weihua Nakamura, Shigeo Rao, Huilan Producer: 20190204 In: PloS one vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2375.	Genome-wide analysis of ETV1 targets: Insights into the role of ETV1 in tumor progression. [electronic resource] by Eid, Wassim Abdel-Rehim, Wafaa Producer: 20200721 In: Journal of cellular biochemistry vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2376.	Identification of a variant associated with early-onset diabetes in the intron of the insulin gene with exome sequencing. [electronic resource] by Matsuno, Shohei Furuta, Hiroto Kosaka, Kitaro Doi, Asako Yorifuji, Tohru Fukuda, Takuya Senmaru, Takafumi Uraki, Shinsuke Matsutani, Norihiko Furuta, Machi Mishima, Hiroyuki Iwakura, Hiroshi Nishi, Masahiro Yoshiura, Kohichiro Fukui, Michiaki Akamizu, Takashi Producer: 20200113 In: Journal of diabetes investigation vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2377.	The genetic basis of Turner syndrome aortopathy. [electronic resource] by Corbitt, Holly Gutierrez, Jacob Silberbach, Michael Maslen, Cheryl L Producer: 20200330 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2378.	Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria. [electronic resource] by Wang, Shengfeng Pitt, Jason J Zheng, Yonglan Yoshimatsu, Toshio F Gao, Guimin Sanni, Ayodele Oluwasola, Olayiwola Ajani, Mustapha Fitzgerald, Dominic Odetunde, Abayomi Khramtsova, Galina Hurley, Ian Popoola, Abiodun Falusi, Adeyinka Ogundiran, Temidayo Obafunwa, John Ojengbede, Oladosu Ibrahim, Nasiru Barretina, Jordi White, Kevin P Huo, Dezheng Olopade, Olufunmilayo I Producer: 20200130 In: International journal of cancer vol. 145 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2379.	Pandora's pregnancy: NIPT, CMA, and genome sequencing-A new era for prenatal genetic testing. [electronic resource] by Hashiloni-Dolev, Yael Nov-Klaiman, Tamar Raz, Aviad Producer: 20200701 In: Prenatal diagnosis vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2380.	Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers. [electronic resource] by Parikh, Aparna R Leshchiner, Ignaty Elagina, Liudmila Goyal, Lipika Levovitz, Chaya Siravegna, Giulia Livitz, Dimitri Rhrissorrakrai, Kahn Martin, Elizabeth E Van Seventer, Emily E Hanna, Megan Slowik, Kara Utro, Filippo Pinto, Christopher J Wong, Alicia Danysh, Brian P de la Cruz, Ferran Fece Fetter, Isobel J Nadres, Brandon Shahzade, Heather A Allen, Jill N Blaszkowsky, Lawrence S Clark, Jeffrey W Giantonio, Bruce Murphy, Janet E Nipp, Ryan D Roeland, Eric Ryan, David P Weekes, Colin D Kwak, Eunice L Faris, Jason E Wo, Jennifer Y Aguet, François Dey-Guha, Ipsita Hazar-Rethinam, Mehlika Dias-Santagata, Dora Ting, David T Zhu, Andrew X Hong, Theodore S Golub, Todd R Iafrate, A John Adalsteinsson, Viktor A Bardelli, Alberto Parida, Laxmi Juric, Dejan Getz, Gad Corcoran, Ryan B Producer: 20191112 In: Nature medicine vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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