Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China

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From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.  
  International journal of pediatric otorhinolaryngology 2017 Jul 98 39-42.
  Pan Jing, Xu Ping, Tang Weibo, Cui Zhongtao, Feng Miao, Wang Chunyi
• Sickle Cell Trait and the Risk of ESRD in Blacks.  
  Journal of the American Society of Nephrology : JASN 2017 Mar .
  Naik Rakhi P, Irvin Marguerite R, Judd Suzanne, Gutiérrez Orlando M, Zakai Neil A, Derebail Vimal K, Peralta Carmen, Lewis Michael R, Zhi Degui, Arnett Donna, McClellan William, Wilson James G, Reiner Alexander P, Kopp Jeffrey B, Winkler Cheryl A, Cushman Ma
• Characteristics of BRCA1/2 mutations carriers including large genomic rearrangements in high risk breast cancer patients.  
  Breast cancer research and treatment 2017 Feb .
  Park Boyoung, Sohn Ji Yeon, Yoon Kyong-Ah, Lee Keun Seok, Cho Eun Hae, Lim Myong Cheol, Yang Moon Jung, Park Soo Jin, Lee Moo Hyun, Lee See Youn, Chang Yoon Jung, Lee Dong Ock, Kong Sun-Young, Lee Eun So
• Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.  
  Journal of molecular medicine (Berlin, Germany) 2017 Jan .
  Villacis Rolando A R, Basso Tatiane R, Canto Luisa M, Pinheiro Maísa, Santiago Karina M, Giacomazzi Juliana, de Paula Cláudia A A, Carraro Dirce M, Ashton-Prolla Patrícia, Achatz Maria I, Rogatto Silvia
• The spectrum of CYP21A2 mutations in Congenital Adrenal Hyperplasia in an Indian cohort.  
  Clinica chimica acta; international journal of clinical chemistry 2017 Jan 464 189-194.
  Khajuria Ragini, Walia Rama, Bhansali Anil, Prasad Rajend

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