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	3461.	Somatic PRKAR1A mutation in sporadic atrial myxoma with cerebral parenchymal metastases: a case report. [electronic resource] by Roque, Ashley Kimbrough, Tara Traner, Christopher Baehring, Joachim M Huttner, Anita Adams, Jennifer Canosa, Sandra Sklar, Jeffrey Madri, Joseph A Producer: 20200522 In: Journal of medical case reports vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3462.	Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance? [electronic resource] by Kause, Franziska Reutter, Heiko Marsch, Florian Thiele, Holger Altmüller, Janine Ludwig, Michael Zhang, Rong Producer: 20180720 In: Molecular medicine reports vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3463.	Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice. [electronic resource] by Tumienė, B Maver, A Writzl, K Hodžić, A Čuturilo, G Kuzmanić-Šamija, R Čulić, V Peterlin, B Producer: 20190925 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3464.	Genomic landscape of ovarian clear cell carcinoma via whole exome sequencing. [electronic resource] by Kim, Se Ik Lee, Ji Won Lee, Maria Kim, Hee Seung Chung, Hyun Hoon Kim, Jae-Weon Park, Noh Hyun Song, Yong-Sang Seo, Jeong-Sun Producer: 20180702 In: Gynecologic oncology vol. 148 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3465.	Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling. [electronic resource] by Richter, Melanie Murtaza, Nadeem Scharrenberg, Robin White, Sean H Johanns, Ole Walker, Susan Yuen, Ryan K C Schwanke, Birgit Bedürftig, Bianca Henis, Melad Scharf, Sarah Kraus, Vanessa Dörk, Ronja Hellmann, Jakob Lindenmaier, Zsuzsa Ellegood, Jacob Hartung, Henrike Kwan, Vickie Sedlacik, Jan Fiehler, Jens Schweizer, Michaela Lerch, Jason P Hanganu-Opatz, Ileana L Morellini, Fabio Scherer, Stephen W Singh, Karun K Calderon de Anda, Froylan Producer: 20200427 In: Molecular psychiatry vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3466.	Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES). [electronic resource] by Liu, Yong Cao, Yu Li, Yaxiong Lei, Dongyun Li, Lin Hou, Zong Liu Han, Shen Meng, Mingyao Shi, Jianlin Zhang, Yayong Wang, Yi Niu, Zhaoyi Xie, Yanhua Xiao, Benshan Wang, Yuanfei Li, Xiao Yang, Lirong Wang, Wenju Jiang, Lihong Producer: 20180906 In: Medical science monitor : international medical journal of experimental and clinical research vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3467.	Novel [electronic resource] by Kaiwar, Charu Zimmermann, Michael T Ferber, Matthew J Niu, Zhiyv Urrutia, Raul A Klee, Eric W Babovic-Vuksanovic, Dusica Producer: 20180101 In: Cold Spring Harbor molecular case studies vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3468.	Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci. [electronic resource] by Westrick, Randal J Tomberg, Kärt Siebert, Amy E Zhu, Guojing Winn, Mary E Dobies, Sarah L Manning, Sara L Brake, Marisa A Cleuren, Audrey C Hobbs, Linzi M Mishack, Lena M Johnston, Alexander J Kotnik, Emilee Siemieniak, David R Xu, Jishu Li, Jun Z Saunders, Thomas L Ginsburg, David Producer: 20180604 In: Proceedings of the National Academy of Sciences of the United States of America vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3469.	A phase 2 study of vorinostat in locally advanced, recurrent, or metastatic adenoid cystic carcinoma. [electronic resource] by Goncalves, Priscila H Heilbrun, Lance K Barrett, Michael T Kummar, Shivaani Hansen, Aaron R Siu, Lillian L Piekarz, Richard L Sukari, Ammar W Chao, Joseph Pilat, Mary Jo Smith, Daryn W Casetta, Lindsay Boerner, Scott A Chen, Alice Lenkiewicz, Elizabeth Malasi, Smriti LoRusso, Patricia M Producer: 20180313 In: Oncotarget vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3470.	Collecting duct carcinoma of the kidney is associated with CDKN2A deletion and SLC family gene up-regulation. [electronic resource] by Wang, Jianmin Papanicolau-Sengos, Antonios Chintala, Sreenivasulu Wei, Lei Liu, Biao Hu, Qiang Miles, Kiersten Marie Conroy, Jeffrey M Glenn, Sean T Costantini, Manuela Magi-Galluzzi, Cristina Signoretti, Sabina Choueiri, Toni Gallucci, Michele Sentinelli, Steno Fazio, Vito M Poeta, Maria Luana Liu, Song Morrison, Carl Pili, Roberto Producer: 20171229 In: Oncotarget vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3471.	Mutation of chromatin regulators and focal hotspot alterations characterize human papillomavirus-positive oropharyngeal squamous cell carcinoma. [electronic resource] by Haft, Sunny Ren, Shuling Xu, Guorong Mark, Adam Fisch, Kathleen Guo, Theresa W Khan, Zubair Pang, John Ando, Mizuo Liu, Chao Sakai, Akihiro Fukusumi, Takahito Califano, Joseph A Producer: 20200406 In: Cancer vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3472.	Hereditary platelet function disorder from [electronic resource] by Yun, Jae Won Lee, Ki-O Jung, Chul Won Oh, Soo-Young Kim, Sun-Hee Choi, Chul Won Kim, Hee-Jin Producer: 20200518 In: Haematologica vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3473.	Association analysis of exome variants and refraction, axial length, and corneal curvature in a European-American population. [electronic resource] by Vergara, Candelaria Bomotti, Samantha M Valencia, Cristian Klein, Barbara E K Lee, Kristine E Klein, Ronald Klein, Alison P Duggal, Priya Producer: 20191007 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3474.	Copenhagen Prospective Personalized Oncology (CoPPO)-Clinical Utility of Using Molecular Profiling to Select Patients to Phase I Trials. [electronic resource] by Tuxen, Ida Viller Rohrberg, Kristoffer Staal Oestrup, Olga Ahlborn, Lise Barlebo Schmidt, Ane Yde Spanggaard, Iben Hasselby, Jane P Santoni-Rugiu, Eric Yde, Christina Westmose Mau-Sørensen, Morten Nielsen, Finn Cilius Lassen, Ulrik Producer: 20200420 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3475.	Genotype-Phenotype Correlations of Dystrophic Epidermolysis Bullosa in India: Experience from a Tertiary Care Centre. [electronic resource] by Yenamandra, Vamsi K Vellarikkal, Shamsudheen K Chowdhury, Madhumita R Jayarajan, Rijith Verma, Ankit Scaria, Vinod Sivasubbu, Sridhar Ray, Subrata Basu Dinda, Amit K Kabra, Madhulika Sharma, Vinod K Sethuraman, Gomathy Producer: 20190128 In: Acta dermato-venereologica vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3476.	A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report. [electronic resource] by Siavrienė, Evelina Petraitytė, Gunda Mikštienė, Violeta Rančelis, Tautvydas Maldžienė, Živilė Morkūnienė, Aušra Byčkova, Jekaterina Utkus, Algirdas Kučinskas, Vaidutis Preikšaitienė, Eglė Producer: 20191202 In: BMC medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3477.	Novel candidates in early-onset familial colorectal cancer. [electronic resource] by Jansen, Anne M L Ghosh, Pradipta Dakal, Tikam C Slavin, Thomas P Boland, C Richard Goel, Ajay Producer: 20210208 In: Familial cancer vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3478.	Somatic mutation signatures in primary liver tumors of workers exposed to ionizing radiation. [electronic resource] by Goerlitz, David S Blancato, Jan Ramesh, Archana Islam, Md Graham, Garrett T Revina, Valentina Kallakury, Bhaskar Zeck, Jay Kirillova, Evgeniya Loffredo, Christopher A Producer: 20201109 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3479.	Defining an embryonal rhabdomyosarcoma endotype. [electronic resource] by Ricker, Cora A Crawford, Kenneth Matlock, Kevin Lathara, Melvin Seguin, Bernard Rudzinski, Erin R Berlow, Noah E Keller, Charles Producer: 20210527 In: Cold Spring Harbor molecular case studies vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3480.	Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis. [electronic resource] by Breuer, Oded Daum, Hagit Cohen-Cymberknoh, Malena Unger, Susanne Shoseyov, David Stepensky, Polina Keller, Baerbel Warnatz, Klaus Kerem, Eitan Producer: 20171120 In: Respiratory medicine vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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