175 related articles for article (PubMed ID: 31807509)
1. 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]
2. 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]
3. Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.
Wang D; Song L; Shen L; Zhang K; Lv Y; Gao M; Ma J; Wan Y; Gai Z; Liu Y
Front Pharmacol; 2021; 12():644352. PubMed ID: 34335240
[No Abstract] [Full Text] [Related]
4. [The characteristic of hereditary spherocytosis related gene mutation in 37 Chinese hereditary spherocytisis patients].
Peng GX; Yang WR; Zhao X; Jin LP; Zhang L; Zhou K; Li Y; Ye L; Li Y; Li JP; Fan HH; Song L; Yang Y; Xiong YZ; Wu ZJ; Wang HJ; Zhang FK
Zhonghua Xue Ye Xue Za Zhi; 2018 Nov; 39(11):898-903. PubMed ID: 30486584
[No Abstract] [Full Text] [Related]
5. Genotype-degree of hemolysis correlation in hereditary spherocytosis.
Shi Y; Li Y; Yang X; Li X; Peng G; Zhao X; Liu X; Zhao Y; Hu J; Hu X; Zhang B; Zhou K; Yang Y; Xiong Y; Li J; Fan H; Yang W; Ye L; Jing L; Zhang L; Zhang F
BMC Genomics; 2023 Jun; 24(1):304. PubMed ID: 37280519
[TBL] [Abstract][Full Text] [Related]
6. Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosis.
Alshomar A; Ahmed AA; Rasheed Z; Alhumaydhi FA; Alsagaby S; Aljohani ASM; Alkhamiss AS; Alghsham R; Althwab SA; Khan MI; Fernández N; Al Abdulmonem W
Nucleosides Nucleotides Nucleic Acids; 2024 Feb; ():1-20. PubMed ID: 38319988
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis.
Wang R; Yang S; Xu M; Huang J; Liu H; Gu W; Zhang X
Sci China Life Sci; 2018 Aug; 61(8):947-953. PubMed ID: 29572776
[TBL] [Abstract][Full Text] [Related]
9. Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.
More TA; Devendra R; Dongerdiye R; Warang P; Kedar P
Mol Genet Genomics; 2023 Mar; 298(2):427-439. PubMed ID: 36598564
[TBL] [Abstract][Full Text] [Related]
10. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
Choi HS; Choi Q; Kim JA; Im KO; Park SN; Park Y; Shin HY; Kang HJ; Kook H; Kim SY; Kim SJ; Kim I; Kim JY; Kim H; Park KD; Park KB; Park M; Park SK; Park ES; Park JA; Park JE; Park JK; Baek HJ; Seo JH; Shim YJ; Ahn HS; Yoo KH; Yoon HS; Won YW; Lee KS; Lee KC; Lee MJ; Lee SA; Lee JA; Lee JM; Lee JH; Lee JW; Lim YT; Jung HJ; Chueh HW; Choi EJ; Jung HL; Kim JH; Lee DS;
Orphanet J Rare Dis; 2019 May; 14(1):114. PubMed ID: 31122244
[TBL] [Abstract][Full Text] [Related]
11. Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China.
Wang X; Zhang A; Huang M; Chen L; Hu Q; Lu Y; Cheng L
Front Genet; 2020; 11():953. PubMed ID: 33014018
[TBL] [Abstract][Full Text] [Related]
12. An
Wang X; Mao L; Shen N; Peng J; Zhu Y; Hu Q; Lu Y
Oncotarget; 2017 Dec; 8(68):113282-113286. PubMed ID: 29348906
[TBL] [Abstract][Full Text] [Related]
13. Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis.
Xie F; Lei L; Cai B; Gan L; Gao Y; Liu X; Zhou L; Jiang J
Mol Genet Genomic Med; 2021 Apr; 9(4):e1577. PubMed ID: 33620149
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel
Wang X; Yi B; Mu K; Shen N; Zhu Y; Hu Q; Lu Y
Oncotarget; 2017 Nov; 8(57):96791-96797. PubMed ID: 29228571
[TBL] [Abstract][Full Text] [Related]
15. Identification of variants in 94 Chinese patients with hereditary spherocytosis by next-generation sequencing.
Wang WJ; Xie JD; Yao H; Ding ZX; Jiang AR; Ma L; Shen HJ; Chen SN
Clin Genet; 2023 Jan; 103(1):67-78. PubMed ID: 36203343
[TBL] [Abstract][Full Text] [Related]
16. Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis.
Guan H; Liang X; Zhang R; Wang H; Liu W; Zhang R; Yang J; Liu S
Hematology; 2018 Jul; 23(6):357-361. PubMed ID: 29099659
[TBL] [Abstract][Full Text] [Related]
17. [Clinical characteristics and genetic analysis of hereditary spherocytosis caused by mutations of ANK1 and SPTB genes].
Gong J; He XL; Zou RY; Chen KK; You YL; Zou H; Tian X; Zhu CG
Zhongguo Dang Dai Er Ke Za Zhi; 2019 Apr; 21(4):370-374. PubMed ID: 31014431
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of
Tian Y; Wang Y; Yang J; Gao P; Xu H; Wu Y; Li M; Chen H; Lu D; Yan H
Front Genet; 2023; 14():1221853. PubMed ID: 37795245
[TBL] [Abstract][Full Text] [Related]
20. [Clinical manifestations of erythrocyte membrane protein coding gene mutations in hereditary spherocytosis].
Sun XJ; Li HY; Li DP; Liu YZ; Zhang JY; Yin YK; Su MH; Pan H; Li QL; Hu B; Liu H; Shi J
Zhonghua Xue Ye Xue Za Zhi; 2018 Nov; 39(11):912-916. PubMed ID: 30486587
[No Abstract] [Full Text] [Related]
[Next] [New Search]