59 related articles for article (PubMed ID: 29505016)
1. Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis.
Bai L; Zheng L; Li B; Huang H; Shi X; Yi Y
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Apr; 48(4):565-574. PubMed ID: 37385619
[TBL] [Abstract][Full Text] [Related]
2. The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis.
Shen H; Gao Z; Ye Q
Genet Test Mol Biomarkers; 2024 Jan; 28(1):33-38. PubMed ID: 38294355
[No Abstract] [Full Text] [Related]
3. Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis.
Xue J; He Q; Xie X; Su A; Cao S
Ann Transl Med; 2019 Oct; 7(20):527. PubMed ID: 31807509
[TBL] [Abstract][Full Text] [Related]
4. Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing.
Jang W; Kim J; Chae H; Kim M; Koh KN; Park CJ; Kim Y
Int J Hematol; 2019 Aug; 110(2):250-254. PubMed ID: 30903564
[TBL] [Abstract][Full Text] [Related]
5. Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs‑negative hemolytic jaundice.
Wang X; Liu A; Lu Y; Hu Q
Mol Med Rep; 2019 Apr; 19(4):2801-2807. PubMed ID: 30816434
[TBL] [Abstract][Full Text] [Related]
6. A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the
Yang K; Ren Q; Wu Y; Zhou Y; Yin X
Hemoglobin; 2019 Mar; 43(2):140-144. PubMed ID: 31190573
[TBL] [Abstract][Full Text] [Related]
7. Current Status of Molecular Diagnosis of Hereditary Hemolytic Anemia in Korea.
Chueh HW; Shim YJ; Jung HL; Kim N; Hwang SM; Kim M; Choi HS;
J Korean Med Sci; 2024 May; 39(18):e162. PubMed ID: 38742293
[TBL] [Abstract][Full Text] [Related]
8. Five Years' Experience with Gene Panel Sequencing in Hereditary Hemolytic Anemia Screened by Routine Peripheral Blood Smear Examination.
Kim N; Kim TY; Han JY; Park J
Diagnostics (Basel); 2023 Feb; 13(4):. PubMed ID: 36832257
[TBL] [Abstract][Full Text] [Related]
9. Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing.
Bogusławska DM; Skulski M; Machnicka B; Potoczek S; Kraszewski S; Kuliczkowski K; Sikorski AF
Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681667
[TBL] [Abstract][Full Text] [Related]
10. Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report.
Du Z; Luo G; Wang K; Bing Z; Pan S
BMC Pediatr; 2021 Jun; 21(1):291. PubMed ID: 34182956
[TBL] [Abstract][Full Text] [Related]
11. A novel
Liu Y; Zheng J; Song L; Fang Y; Sun C; Li N; Liu G; Shu J
Exp Ther Med; 2020 Oct; 20(4):3253-3259. PubMed ID: 32855695
[TBL] [Abstract][Full Text] [Related]
12. Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil.
Svidnicki MCCM; Zanetta GK; Congrains-Castillo A; Costa FF; Saad STO
Ann Hematol; 2020 May; 99(5):955-962. PubMed ID: 32266426
[TBL] [Abstract][Full Text] [Related]
13. Targeted next-generation sequencing identifies a novel nonsense mutation in SPTB for hereditary spherocytosis: A case report of a Korean family.
Shin S; Jang W; Kim M; Kim Y; Park SY; Park J; Yang YJ
Medicine (Baltimore); 2018 Jan; 97(3):e9677. PubMed ID: 29505016
[TBL] [Abstract][Full Text] [Related]
14. Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis.
Fan LL; Liu JS; Huang H; Du R; Xiang R
J Gene Med; 2019 Feb; 21(2-3):e3073. PubMed ID: 30690801
[TBL] [Abstract][Full Text] [Related]
15. Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing.
Qin L; Nie Y; Zhang H; Chen L; Zhang D; Lin Y; Ru K
J Hum Genet; 2020 Apr; 65(4):427-434. PubMed ID: 31980736
[TBL] [Abstract][Full Text] [Related]
16. A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.
Li S; Guo P; Mi L; Chai X; Xi K; Liu T; Lu L; Li J
Ann Hematol; 2022 Apr; 101(4):731-738. PubMed ID: 35099593
[TBL] [Abstract][Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]