Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Anemia and SPTB[original query] |
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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 |
Three Novel Spectrin Variants in Jaundiced Neonates. Clinical pediatrics 2017 1 57 (1): 19-26. Christensen Robert D, Agarwal Archana M, Yaish Hassan M, Reading N Scott, O'Brien Elizabeth A, Prchal Josef |
[Clinical manifestations of erythrocyte membrane protein coding gene mutations in hereditary spherocytosis]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2018 11 39 (11): 912-916. Sun X J, Li H Y, Li D P, Liu Y Z, Zhang J Y, Yin Y K, Su M H, Pan H, Li Q L, Hu B, Liu H, Shi |
Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan. Clinica chimica acta; international journal of clinical chemistry 2018 Dec 487 311-317. Lin Pei-Chin, Chiou Shyh-Shin, Lin Chien-Yu, Wang Shu-Chen, Huang Hsi-Yuan, Chang Ya-Sian, Tseng Yu-Hsin, Kan Tzu-Min, Liao Yu-Mei, Tsai Shih-Pien, Peng Ching-Tien, Chang Jan-Gow |
Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China. Frontiers in genetics 2020 10 11 953. Wang Xiong, Zhang Ai, Huang Ming, Chen Li, Hu Qun, Lu Yanjun, Cheng Limi |
Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing. Journal of human genetics 2020 1 65 (4): 427-434. Qin Li, Nie Yanbo, Zhang Hong, Chen Long, Zhang Donglei, Lin Yani, Ru K |
Preliminary Study on the Clinical and Genetic Characteristics of Hereditary Spherocytosis in 15 Chinese Children. Frontiers in genetics 2021 4 12 652376. Wu Chongjun, Xiong Ting, Xu Zhongjin, Zhan Chunlei, Chen Feng, Ye Yao, Wang Hong, Yang |
Literature review on genotype-phenotype correlation in patients with hereditary spherocytosis. Clinical genetics 2022 Sep . Yang Liqing, Shu Huiying, Zhou Min, Gong Yupi |
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis. Genetic testing and molecular biomarkers 2022 5 26 (5): 270-276. Herrera-Tirado Isis Mariela, Espinoza-Mata Laura Lucia, Rizo-delaTorre Lourdes Del Carmen, Becerra-Solano Luis Eduardo, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javi |
Genotype-degree of hemolysis correlation in hereditary spherocytosis. BMC genomics 2023 6 24 (1): 304. Yimeng Shi, Yuan Li, Xiawan Yang, Xiaoxia Li, Guangxin Peng, Xin Zhao, Xu Liu, Yufei Zhao, Jing Hu, Xiangrong Hu, Baohang Zhang, Kang Zhou, Yang Yang, Youzhen Xiong, Jianping Li, Huihui Fan, Wenrui Yang, Lei Ye, Liping Jing, Li Zhang, Fengkui Zha |
Case report: Whole-exome sequencing for a hereditary elliptocytosis case with an unexpectedly low HbA. Frontiers in medicine 2023 12 10 1301760. Lu Pang, Ziyi Zeng, Yadi Ding, Haiming Huang, Haixia |
Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry. Annals of hematology 2023 11 . Duantida Songdej, Pacharapan Surapolchai, Patcharee Komwilaisak, Pornpun Sripornsawan, Supanun Lauhasurayotin, Nattiya Teawtrakul, Tarinee Rungjirajittranon, Adisak Tantiworawit, Phakatip Sinlapamongkolkul, Kitti Torcharus, Pranee Sutcharitchan, Bunchoo Pongtanakul, Nongnuch Sirachainan, Pimlak Charoenkw |
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- Page last updated:Apr 16, 2024
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