Mo QH - Search Results

1

Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital.

Liao C, Mo QH, Li J, Li LY, Huang YN, Hua L, Li QM, Zhang JZ, Feng Q, Zeng R, Zhong HZ, Jia SQ, Cui YY, Xu XM. Liao C, et al. Among authors: mo qh. Prenat Diagn. 2005 Feb;25(2):163-71. doi: 10.1002/pd.1079. Prenat Diagn. 2005. PMID: 15712323

2

[A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].

Zhou YQ, Mo QH, Lu JH, Li LY, Liang X, Jia SQ, Xiao GF, Zhou WJ, Xiao QZ, Xu XM. Zhou YQ, et al. Among authors: mo qh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Jun;25(3):256-61. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18543211 Chinese.

3

Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.

Tan JR, Li WJ, Ma JY, Mo QH, Li LY, Jia SQ, Lao XW, Li LY, He RQ, Xu XM. Tan JR, et al. Among authors: mo qh. Di Yi Jun Yi Da Xue Xue Bao. 2003 Jul;23(7):716-9. Di Yi Jun Yi Da Xue Xue Bao. 2003. PMID: 12865230

4

[Rapid diagnosis of non-deletion alpha-thalassemias by reverse dot blot].

Li LY, Mo QH, Xu XM. Li LY, et al. Among authors: mo qh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):345-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12903049 Chinese.

5

[A rare transcription mutation (-90 C-->T) in a Chinese family with beta-thalassemia].

Li WJ, Lao XW, Jai SQ, Liang FA, Mo QH, Ma JY, Xu XM. Li WJ, et al. Among authors: mo qh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Dec;20(6):468-70. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14669211 Chinese.

6

[Accurate and rapid prenatal diagnosis of beta-thalassemia by a multiplex primer extension and denaturing high-performance liquid chromatography technique].

Hua L, Zhu H, Li XR, Li J, Mo QH, Liao C, Hou YX, Zhong M, Xu XM. Hua L, et al. Among authors: mo qh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):600-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583991 Chinese.

7

Reliable and high-throughput mutation screening for beta-thalassemia by a single-base extension/fluorescence polarization assay.

Mo QH, Zhu H, Li LY, Xu XM. Mo QH, et al. Genet Test. 2004 Fall;8(3):257-62. doi: 10.1089/gte.2004.8.257. Genet Test. 2004. PMID: 15727248

8

A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.

Chen XW, Mo QH, Li Q, Zeng R, Xu XM. Chen XW, et al. Among authors: mo qh. Ann Hematol. 2007 Sep;86(9):653-7. doi: 10.1007/s00277-007-0312-8. Epub 2007 May 22. Ann Hematol. 2007. PMID: 17516066

9

[A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].

Li Q, Li LY, Mo QH. Li Q, et al. Among authors: mo qh. Nan Fang Yi Ke Da Xue Xue Bao. 2008 Jan;28(1):16-9. Nan Fang Yi Ke Da Xue Xue Bao. 2008. PMID: 18227017 Chinese.

10

Rapid, accurate genotyping of the common -alpha(4.2) thalassaemia deletion based on the use of denaturing HPLC.

Ou-Yang H, Hua L, Mo QH, Xu XM. Ou-Yang H, et al. Among authors: mo qh. J Clin Pathol. 2004 Feb;57(2):159-63. doi: 10.1136/jcp.2003.011130. J Clin Pathol. 2004. PMID: 14747441 Free PMC article.

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