Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Counseling and ANK1[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 |
| 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 |
- Page last reviewed:Feb 1, 2024
- Content source: