Similar articles for PMID: 31980736

Year	Number of Results
1992	1
1993	1
1994	1
1995	1
1996	5
1997	5
1998	7
1999	5
2000	4
2001	2
2002	2
2003	3
2004	3
2005	3
2006	2
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2010	4
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2012	3
2013	6
2014	6
2015	5
2016	2
2017	6
2018	14
2019	20
2020	20
2021	19
2022	26
2023	16
2024	0

1

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. Qin L, et al. J Hum Genet. 2020 Apr;65(4):427-434. doi: 10.1038/s10038-020-0724-z. Epub 2020 Jan 24. J Hum Genet. 2020. PMID: 31980736 Clinical Trial.

2

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. Wang R, et al. Sci China Life Sci. 2018 Aug;61(8):947-953. doi: 10.1007/s11427-017-9232-6. Epub 2018 Mar 19. Sci China Life Sci. 2018. PMID: 29572776

3

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. Park J, et al. Clin Genet. 2016 Jul;90(1):69-78. doi: 10.1111/cge.12749. Epub 2016 Mar 15. Clin Genet. 2016. PMID: 26830532

4

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. Wang D, et al. Front Pharmacol. 2021 Jul 16;12:644352. doi: 10.3389/fphar.2021.644352. eCollection 2021. Front Pharmacol. 2021. PMID: 34335240 Free PMC article.

5

[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. Gong J, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Apr;21(4):370-374. doi: 10.7499/j.issn.1008-8830.2019.04.013. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31014431 Free PMC article. Chinese.

6

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. Hao L, et al. J Cell Mol Med. 2019 Jun;23(6):4454-4463. doi: 10.1111/jcmm.14343. Epub 2019 Apr 23. J Cell Mol Med. 2019. PMID: 31016877 Free PMC article.

7

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; Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology. Choi HS, et al. Orphanet J Rare Dis. 2019 May 23;14(1):114. doi: 10.1186/s13023-019-1070-0. Orphanet J Rare Dis. 2019. PMID: 31122244 Free PMC article.

8

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. Wang X, et al. Front Genet. 2020 Aug 18;11:953. doi: 10.3389/fgene.2020.00953. eCollection 2020. Front Genet. 2020. PMID: 33014018 Free PMC article.

9

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. Fan LL, et al. J Gene Med. 2019 Feb;21(2-3):e3073. doi: 10.1002/jgm.3073. Epub 2019 Feb 11. J Gene Med. 2019. PMID: 30690801

10

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. Xie F, et al. Mol Genet Genomic Med. 2021 Apr;9(4):e1577. doi: 10.1002/mgg3.1577. Epub 2021 Feb 23. Mol Genet Genomic Med. 2021. PMID: 33620149 Free PMC article.

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