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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Counseling and SPTB[original query]
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
Multigene Panel Testing Revealed Novel Variants in Hereditary Spherocytosis Patients in Türkiye.
Turkish journal of haematology : official journal of Turkish Society of Haematology 2025 1 .
Ömer Do?ru, Ceren Alavanda, ?enol Demir, Ahmet Koç, P?nar A
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