Xu XM - Search Results

1

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

Sun SC, Ma D, Li MY, Zhang RX, Huang C, Huang HJ, Xie YZ, Wang ZJ, Liu J, Cai DC, Liu CX, Yang Q, Bao FX, Gong XL, Li JR, Hui Z, Wei XF, Zhong JM, Zhou WJ, Shang X, Zhang C, Liu XG, Tang BS, Xiong F, Xu XM. Sun SC, et al. Among authors: xu xm. Brain. 2019 Aug 1;142(8):2215-2229. doi: 10.1093/brain/awz151. Brain. 2019. PMID: 31199454

2

[Molecular screening and prenatal diagnosis of the deletional alpha-thalassemia by polymerase chain reaction amplification].

Xu XM, Cai XH, Li J. Xu XM, et al. Zhonghua Yi Xue Za Zhi. 1994 Aug;74(8):495-7, 520. Zhonghua Yi Xue Za Zhi. 1994. PMID: 7994662 Chinese.

3

[Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda].

Zhou WJ, Zhou SY, Huang SW, Zhou JP, Xu XM. Zhou WJ, et al. Among authors: xu xm. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):15-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18247296 Chinese.

4

Rapid genotyping of known mutations and polymorphisms in beta-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes.

Li Q, Li LY, Huang SW, Li L, Chen XW, Zhou WJ, Xu XM. Li Q, et al. Among authors: xu xm. Clin Biochem. 2008 Jun;41(9):681-7. doi: 10.1016/j.clinbiochem.2008.02.008. Epub 2008 Feb 21. Clin Biochem. 2008. PMID: 18339318

5

SYBR Green-based real-time PCR assay for detection of VKORC1 and CYP2C9 polymorphisms that modulate warfarin dose requirement.

Huang SW, Li Q, Zhu SY, Li L, Xiong F, Jia YK, Xu XM. Huang SW, et al. Among authors: xu xm. Clin Chem Lab Med. 2009;47(1):26-31. doi: 10.1515/CCLM.2009.008. Clin Chem Lab Med. 2009. PMID: 19117406

6

Development and validation of a zeta-globin-specific ELISA for carrier screening of the (--SEA) alpha thalassaemia deletion.

Tang L, Zhu P, Zhou WJ, Zheng J, Zhou YQ, Fu N, Xu XM. Tang L, et al. Among authors: xu xm. J Clin Pathol. 2009 Feb;62(2):147-51. doi: 10.1136/jcp.2008.059477. J Clin Pathol. 2009. PMID: 19181632

7

The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity.

Chen W, Zhang X, Shang X, Cai R, Li L, Zhou T, Sun M, Xiong F, Xu X. Chen W, et al. BMC Med Genet. 2010 Feb 25;11:31. doi: 10.1186/1471-2350-11-31. BMC Med Genet. 2010. PMID: 20181291 Free PMC article.

8

Molecular characterization of SMN copy number derived from carrier screening and from core families with SMA in a Chinese population.

Sheng-Yuan Z, Xiong F, Chen YJ, Yan TZ, Zeng J, Li L, Zhang YN, Chen WQ, Bao XH, Zhang C, Xu XM. Sheng-Yuan Z, et al. Among authors: xu xm. Eur J Hum Genet. 2010 Sep;18(9):978-84. doi: 10.1038/ejhg.2010.54. Epub 2010 May 5. Eur J Hum Genet. 2010. PMID: 20442745 Free PMC article.

9

Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern China.

Wang Z, Yu W, Li Y, Shang X, Zhang X, Xiong F, Xu X. Wang Z, et al. Blood Cells Mol Dis. 2010 Aug 15;45(2):128-32. doi: 10.1016/j.bcmd.2010.04.005. Blood Cells Mol Dis. 2010. PMID: 20627634

10

Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.

Lou JW, Li Q, Wei XF, Huang JW, Xu XM. Lou JW, et al. Among authors: xu xm. Hemoglobin. 2010;34(4):343-53. doi: 10.3109/03630269.2010.486357. Hemoglobin. 2010. PMID: 20642332

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,003 results

Search Page

Filters