159 related articles for article (PubMed ID: 35218326)
1. Identification of a novel ANK1 mutation in hereditary spherocytosis co-existing with BWS.
Zhang Q; Zhang C; Wang Y; Hao S; Shi J; Feng X; Zheng L; Wang X; Xue C; Zhou B; Liu F; Zhao F; Li X; Deng L; Hou J; Meng Z
Mol Genet Genomic Med; 2022 Apr; 10(4):e1903. PubMed ID: 35218326
[TBL] [Abstract][Full Text] [Related]
2. Spectrum of Ankyrin Mutations in Hereditary Spherocytosis: A Case Report and Review of the Literature.
Luo Y; Li Z; Huang L; Tian J; Xiong M; Yang Z
Acta Haematol; 2018; 140(2):77-86. PubMed ID: 30227413
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A Novel
Jang W; Kim SK; Nahm CH; Choi JW; Kim JJ; Moon Y
Ann Clin Lab Sci; 2021 Jan; 51(1):136-139. PubMed ID: 33653793
[TBL] [Abstract][Full Text] [Related]
5. A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis.
Li J; Guo H; Zhu Z; Sun J
Acta Haematol; 2022; 145(6):575-581. PubMed ID: 35817016
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report.
Chai S; Jiao R; Sun X; Fu P; Zhao Q; Sang M
BMC Med Genet; 2020 Nov; 21(1):223. PubMed ID: 33187473
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.
Han JH; Kim S; Jang H; Kim SW; Lee MG; Koh H; Lee JH
PLoS One; 2015; 10(6):e0131251. PubMed ID: 26107955
[TBL] [Abstract][Full Text] [Related]
10. A de novo ANK1 mutation associated to hereditary spherocytosis: a case report.
Huang TL; Sang BH; Lei QL; Song CY; Lin YB; Lv Y; Yang CH; Li N; Yang YH; Zhang XW; Tian X
BMC Pediatr; 2019 Feb; 19(1):62. PubMed ID: 30777044
[TBL] [Abstract][Full Text] [Related]
11. Beckwith-Wiedemann syndrome with long QT caused by a deletion involving KCNQ1 but not KCNQ1OT1:TSS-DMR.
Urakawa T; Ozawa J; Tanaka M; Narusawa H; Matsuoka K; Fukami M; Nagasaki K; Kagami M
Eur J Med Genet; 2023 Jan; 66(1):104671. PubMed ID: 36402267
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
[TBL] [Abstract][Full Text] [Related]
14. A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.
Zhu F; Liang M; Xu L; Peng Z; Cai D; Wei X; Lin L; Shang X
Gene; 2020 Feb; 726():144226. PubMed ID: 31669644
[TBL] [Abstract][Full Text] [Related]
15. Targeted next-generation sequencing identified a novel
Sun Q; Xie Y; Wu P; Li S; Hua Y; Lu X; Zhao W
Hematology; 2019 Dec; 24(1):583-587. PubMed ID: 31390973
[No Abstract] [Full Text] [Related]
16. Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
Park J; Jeong DC; Yoo J; Jang W; Chae H; Kim J; Kwon A; Choi H; Lee JW; Chung NG; Kim M; Kim Y
Clin Genet; 2016 Jul; 90(1):69-78. PubMed ID: 26830532
[TBL] [Abstract][Full Text] [Related]
17. High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
Baskin B; Choufani S; Chen YA; Shuman C; Parkinson N; Lemyre E; Micheil Innes A; Stavropoulos DJ; Ray PN; Weksberg R
Hum Genet; 2014 Mar; 133(3):321-30. PubMed ID: 24154661
[TBL] [Abstract][Full Text] [Related]
18. Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
Hao L; Li S; Ma D; Chen S; Zhang B; Xiao D; Zhang J; Jiang N; Jiang S; Ma J
J Cell Mol Med; 2019 Jun; 23(6):4454-4463. PubMed ID: 31016877
[TBL] [Abstract][Full Text] [Related]
19. Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reportsĀ and review of the literature.
Xie L; Xing Z; Li C; Liu SX; Wen FQ
BMC Med Genomics; 2021 Mar; 14(1):77. PubMed ID: 33706756
[TBL] [Abstract][Full Text] [Related]
20. De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing.
Wang Y; Huang L; Zhu Y; An X; Li J; Zhen J; Yu J
BMC Pediatr; 2023 Jan; 23(1):23. PubMed ID: 36647015
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]