Ren Z - Search Results

1

[Current status and trends of prenatal gene diagnosis].

Ren Z, Zeng Y. Ren Z, et al. Zhonghua Fu Chan Ke Za Zhi. 1997 Nov;32(11):643-5. Zhonghua Fu Chan Ke Za Zhi. 1997. PMID: 9639760 Chinese. No abstract available.

2

Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria.

Huang SZ, Ren ZR, Zeng YT. Huang SZ, et al. Among authors: ren zr. J Med Genet. 1990 Jan;27(1):65-6. doi: 10.1136/jmg.27.1.65. J Med Genet. 1990. PMID: 1968515 Free PMC article. No abstract available.

3

A new silent mutation found in the Chinese PAH locus and its role in the prenatal diagnosis of phenylketonuria.

Huang SZ, Zhou XD, Ren ZR, Zeng YT, Woo SL. Huang SZ, et al. Among authors: ren zr. Sci China B. 1991 May;34(5):606-10. Sci China B. 1991. PMID: 2059324

4

Prenatal detection of an Arg----Ter mutation at codon 111 of the PAH gene using DNA amplification.

Huang SZ, Zhou XD, Ren ZR, Zeng YT, Woo SL. Huang SZ, et al. Among authors: ren zr. Prenat Diagn. 1990 May;10(5):289-93. doi: 10.1002/pd.1970100503. Prenat Diagn. 1990. PMID: 1975096

5

Prenatal diagnosis of haemophilia B in the first trimester.

Zeng YT, Zhang ML, Ren ZR, Chen SR, Wang HL, Wang ZY, Tong JH. Zeng YT, et al. Among authors: ren zr. J Med Genet. 1987 Oct;24(10):632. doi: 10.1136/jmg.24.10.632. J Med Genet. 1987. PMID: 3681910 Free PMC article. No abstract available.

6

[Suppression of enhanced green fluorescent protein expression in cells by RNA interference].

Xie SY, Zhang JZ, Huang SZ, Ren ZR, Zeng YT. Xie SY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):431-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086284 Chinese.

7

[Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)].

Chen M, Han JY, Sun Q, Kim IH, Ren Z, Huang S, Zeng Y. Chen M, et al. Among authors: ren z. Zhonghua Xue Ye Xue Za Zhi. 2000 Apr;21(4):195-7. Zhonghua Xue Ye Xue Za Zhi. 2000. PMID: 11876981 Chinese.

8

Molecular diagnosis of hemophilia A in Chinese patients by an analysis of inversions in the factor VIII gene.

Chen YD, Zhang YZ, Wu JS, Wang HL, Shao HZ, Ren ZR, Chen Z, Wang ZY, Zeng YT. Chen YD, et al. Among authors: ren zr. Hematopathol Mol Hematol. 1996;10(1-2):63-7. Hematopathol Mol Hematol. 1996. PMID: 8792148

9

Prenatal Diagnosis of β-Thalassemia Using Multiplex Allele-Specific Amplification (MASPCR) in Chinese Families.

Mao YH, Sheng M, Chen MJ, Ren ZR, Zeng YT, Huang SZ. Mao YH, et al. Among authors: ren zr. Hematology. 1996;1(3):253-7. doi: 10.1080/10245332.1996.11746312. Hematology. 1996. PMID: 27406620 Free article.

10

Study of the RNA splicing defect in the common Chinese beta-thalassemia gene, IVS-II nt. 654 C-->T by using mRNA/PCR.

Huang SZ, Ren ZR, Zeng YT, Zeng FY, Rodgers GP, Schecter AN. Huang SZ, et al. Among authors: ren zr. Sci China B. 1992 Oct;35(10):1232-7. Sci China B. 1992. PMID: 1285849

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