Peter Lee-Wright (2010) The Documentary Handbook by Wes Skolits

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Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) by Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Wilfred H S Wong, Mandy H Y Tsang, Mullin H C Yu, Steven L C Pei, K S Yeung, Gary T K Mok, C P Lee, Amelia P W Hui, Mary H Y Tang, Kelvin Y K Chan, Anthony P Y Liu, Wanling Yang, P C Sham, Anita S Y Kan, Brian H Y Chung

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P591: Assessing the performance of automated HPO term extraction for deep phenotyping of patients receiving WES/WGS in a clinical diagnostic laboratory by Kai Lee Yap, Anthony Wong, Sachleen Tuteja, Andrew Skol, Andy Drackley, Alexander Ing, Eleanor Hilton, Michael Carroll, Christopher McCabe, Sabah Kadri, Pamela Rathbun, Katrin Leuer, Joel Charrow

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Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Varian... by Yu-Rong Lee, Yu-Rong Lee, Yu-Chen Lin, Yu-Chen Lin, Yi-Han Chang, Yi-Han Chang, Hsin-Yu Huang, Yi-Kai Hong, Yi-Kai Hong, Wilson Jr F. Aala, Wei-Ting Tu, Meng-Che Tsai, Yen-Yin Chou, Chao-Kai Hsu, Chao-Kai Hsu, Chao-Kai Hsu

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Modelling the impact of trapped lee waves on offshore wind farm power output by S. J. Ollier, S. J. Watson

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A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study by Syuan-Yu Hong, Jiann-Jou Yang, Shuan-Yow Li, Inn-Chi Lee

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Genomic Analysis of Korean Patient With Microcephaly by Jiwon Lee, Jong Eun Park, Chung Lee, Ah Reum Kim, Byung Joon Kim, Woong-Yang Park, Chang-Seok Ki, Jeehun Lee

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A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family by Kausar, Mehran, Chew, Elaine Guo Yan, Ullah, Hazrat, Anees, Mariam, Khor, Chiea Chuen, Foo, Jia Nee, Makitie, Outi, Siddiqi, Saima

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The Modified Shields Classification and 12 Families with Defined <i>DSPP</i> Mutations by James P. Simmer, Hong Zhang, Sophie J. H. Moon, Lori A-J. Donnelly, Yuan-Ling Lee, Figen Seymen, Mine Koruyucu, Hui-Chen Chan, Kevin Y. Lee, Suwei Wu, Chia-Lan Hsiang, Anthony T. P. Tsai, Rebecca L. Slayton, Melissa Morrow, Shih-Kai Wang, Edward D. Shields, Jan C.-C. Hu

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A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family by Mehran Kausar, Mehran Kausar, Mehran Kausar, Elaine Guo Yan Chew, Elaine Guo Yan Chew, Hazrat Ullah, Mariam Anees, Chiea Chuen Khor, Jia Nee Foo, Jia Nee Foo, Outi Makitie, Outi Makitie, Saima Siddiqi

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Frontofacial Features of Unilateral Lambdoid Craniosynostosis: A Multicenter Assessment by Jonathan Lee, MD, Sanjay Naran, MD, Daniel Mazzaferro, MD, Ari Wes, MD, Erin E. Anstadt, MD, Jesse Taylor, MD, Jesse Goldstein, MD, Scott Bartlett, MD, Joseph Losee, MD

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1079 Type I interferon regulation by USP18 is a key vulnerability in cancer by Feng Wang, Bing Yang, Benedikt M Kessler, Veronica Jove, Heather Wheeler, Chiachin Wilson Lee, David R Healy, Kymberly Levine, Erik C Ralph, Anand Giddabasappa, Paula Loria, Masaya Yamaguchi, Agustin Casimiro-Garcia, Adan Pinto-Fernandez, Veronique Frattini, Paul Wes

Metatranscriptomics analysis reveals a novel transcriptional and translational landscape during Middle East respiratory syndrome coronavirus infection by Ethan J. Fritch, Wes Sanders, Amy C. Sims, Laura E. Herring, Natalie K. Barker, Athena A. Schepmoes, Karl K. Weitz, Jordan R. Texier, Dirk P. Dittmer, Lee M. Graves, Richard D. Smith, Katrina M. Waters, Nathaniel J. Moorman, Ralph S. Baric, Rachel L. Graham

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Type I interferon regulation by USP18 is a key vulnerability in cancer by Jové, V, Wheeler, H, Lee, CW, Healy, DR, Levine, K, Ralph, EC, Yamaguchi, M, Jiang, ZK, Cabral, E, Xu, Y, Stock, J, Yang, B, Giddabasappa, A, Loria, P, Casimiro-Garcia, A, Kessler, BM, Pinto-Fernández, A, Frattini, V, Wes, PD, Wang, F

The incorporation of next-generation sequencing into pediatric care by Ni-Chung Lee

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Type I interferon regulation by USP18 is a key vulnerability in cancer by Veronica Jové, Heather Wheeler, Chiachin Wilson Lee, David R. Healy, Kymberly Levine, Erik C. Ralph, Masaya Yamaguchi, Ziyue Karen Jiang, Edward Cabral, Yingrong Xu, Jeffrey Stock, Bing Yang, Anand Giddabasappa, Paula Loria, Agustin Casimiro-Garcia, Benedikt M. Kessler, Adán Pinto-Fernández, Véronique Frattini, Paul D. Wes, Feng Wang

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Genetic Characteristics Associated With Drug Resistance in Lung Cancer and Colorectal Cancer Using Whole Exome Sequencing of Cell-Free DNA by Jong Won Lee, Jong Won Lee, Jong Won Lee, Young Soo Park, Jung Yoon Choi, Won Jin Chang, Soohyeon Lee, Jae Sook Sung, Boyeon Kim, Boyeon Kim, Saet Byeol Lee, Saet Byeol Lee, Sung Yong Lee, Jungmin Choi, Jungmin Choi, Yeul Hong Kim, Yeul Hong Kim, Yeul Hong Kim

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Read Count Patterns and Detection of Cancerous Copy Number Alterations in Plasma Cell-Free DNA Whole Exome Sequencing Data for Advanced Non-Small Cell Lung Cancer by Ho Jang, Chang-Min Choi, Seung-Hyeun Lee, Sungyong Lee, Mi-Kyung Jeong

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Molecular Characterization and Putative Pathogenic Pathways of Tuberous Sclerosis Complex–Associated Renal Cell Carcinoma by Jeong Hwan Park, Cheol Lee, Mee Soo Chang, Kwangsoo Kim, Seongmin Choi, Hyunjung Lee, Hyun-Seob Lee, Kyung Chul Moon

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Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability by Ji Yoon Han, In Goo Lee

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