HuGE Literature Finder
Records 1-8
[Application of High Resolution Melting Curve Analysis in Detection of SLC4A1 Gene Mutation in Patients with Hereditary Spherocytosis].
Zhongguo shi yan xue ye xue za zhi 2018 Dec 26 (6): 1826-1830. Ma Shi-Yue, Liao Lin, He Ben-Jin, Lin Fa-Qu |
[Identification of a novel ANK1 gene mutation in a newborn with hereditary spherocytosis].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Feb 33 (1): 44-7. Jiang Min, Lu Jie, Zhong Yan, Wang Yajuan, Yang Caiy |
Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
Clinical genetics 2016 Feb . Park Joonhong, Jeong Dae-Chul, Yoo Jaeeun, Jang Woori, Chae Hyojin, Kim Jiyeon, Kwon Ahlm, Choi Hayoung, Lee Jae-Wook, Chung Nack-Gyun, Kim Myungshin, Kim Yongg |
[Hereditary red cell membrane disorders in Japan: comparison with other countries].
[Rinsho? ketsueki] The Japanese journal of clinical hematology 2015 Jul 56 (7): 760-70. Nakanishi Hidekazu, Wada Hideho, Suemori Shinichiro, Sugihara Takas |
Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humans.
![]() PloS one 2013 8 (7): e69206. Pistis Giorgio, Okonkwo Shawntel U, Traglia Michela, Sala Cinzia, Shin So-Youn, Masciullo Corrado, Buetti Iwan, Massacane Roberto, Mangino Massimo, Thein Swee-Lay, Spector Timothy D, Ganesh Santhi, , Pirastu Nicola, Gasparini Paolo, Soranzo Nicole, Camaschella Clara, Hart Daniel, Green Michael R, Toniolo Danie |
[Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis].
Gaceta médica de México 0 142 (5): 435-7. Camacho-Torres Ana Luisa, Sánchez-López Josefina Yoaly, Mesa-Cornejo Viviana Matilde, Ibarra Bertha, Perea-Díaz Francisco Javi |
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