Genetic Counseling - https://phgkb.cdc.gov/GAPPKB/phgHome.do

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

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

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• 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
• An insertion/deletion polymorphism within 3'UTR of RYR2 modulates sudden unexplained death risk in Chinese populations.  
  Forensic science international 2017 Jan 270 165-172.
  Wang Shouyu, Zhang Zhixiang, Yang Ya, Wang Chaoqun, Tao Ruiyang, Hu Shuxiang, Yin Zhixia, Zhang Qing, Li Lijuan, He Yan, Zhu Shaohua, Li Chengtao, Zhang Suhua, Zhang Jianhua, Sheng Lihui, Wu Fangyu, Luo Bin, Gao Yuzh
• 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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