Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Counseling and SPTB[original query] |
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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 |
Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis. Annals of translational medicine 2019 12 7 (20): 527. Xue Jun, He Qing, Xie Xiaojing, Su Ailing, Cao Shib |
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 |
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- Page last updated:Apr 22, 2024
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