44 related articles for article (PubMed ID: 29099659)
21. 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]
22. 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]
23. 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]
24. 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]
25. 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]
26. Literature review on genotype-phenotype correlation in patients with hereditary spherocytosis.
Yang L; Shu H; Zhou M; Gong Y
Clin Genet; 2022 Dec; 102(6):474-482. PubMed ID: 36071563
[TBL] [Abstract][Full Text] [Related]
27. [Molecular mechanism of hereditary spherocytosis].
Bogusławska DM; Heger E; Sikorski AF
Pol Merkur Lekarski; 2006 Jan; 20(115):112-6. PubMed ID: 16617750
[TBL] [Abstract][Full Text] [Related]
28. Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives.
He BJ; Liao L; Deng ZF; Tao YF; Xu YC; Lin FQ
Acta Haematol; 2018; 139(1):60-66. PubMed ID: 29402830
[TBL] [Abstract][Full Text] [Related]
29. A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial features.
Miya K; Shimojima K; Sugawara M; Shimada S; Tsuri H; Harai-Tanaka T; Nakaoka S; Kanegane H; Miyawaki T; Yamamoto T
Gene; 2012 Sep; 506(1):146-9. PubMed ID: 22771917
[TBL] [Abstract][Full Text] [Related]
30. Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
Da Costa L; Galimand J; Fenneteau O; Mohandas N
Blood Rev; 2013 Jul; 27(4):167-78. PubMed ID: 23664421
[TBL] [Abstract][Full Text] [Related]
31. Hereditary spherocytosis: from clinical to molecular defects.
Iolascon A; Miraglia del Giudice E; Perrotta S; Alloisio N; Morlé L; Delaunay J
Haematologica; 1998 Mar; 83(3):240-57. PubMed ID: 9573679
[TBL] [Abstract][Full Text] [Related]
32. Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis.
Delaunay J; Alloisio N; Morle L; Baklouti F; Dalla Venezia N; Maillet P; Wilmotte R
Ann Genet; 1996; 39(4):209-21. PubMed ID: 9037349
[TBL] [Abstract][Full Text] [Related]
33. [Hereditary spherocytosis].
Ideguchi H
Nihon Rinsho; 1996 Sep; 54(9):2478-83. PubMed ID: 8890582
[TBL] [Abstract][Full Text] [Related]
34. [Diagnosis and therapy of hemolytic anemia--genetic analysis and membrane protein deficiency in hereditary spherocytosis].
Kanzaki A; Kaku M; Yawata Y
Nihon Naika Gakkai Zasshi; 1999 Jun; 88(6):1003-9. PubMed ID: 10465942
[No Abstract] [Full Text] [Related]
35. A Systematic review on diagnostic methods of red cell membrane disorders in Asia.
Silva R; Amarasinghe D; Perera S; Premawardhena A
Int J Lab Hematol; 2022 Apr; 44(2):248-262. PubMed ID: 35068068
[TBL] [Abstract][Full Text] [Related]
36. 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]
37.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
38.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
39.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
