Gu XF - Search Results

1

[Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis].

Qiu WJ, Zhang YF, Pan J, Ye J, Liu XQ, Han LS, Gu XF. Qiu WJ, et al. Among authors: gu xf. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):44-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696478 Chinese.

2

Screening for tetrahydrobiopterin deficiency among hyperphenylalaninemia patients in Southern China.

Ye J, Liu X, Ma X, Zhang Y, Huang X, Chen R, Gu X. Ye J, et al. Chin Med J (Engl). 2002 Feb;115(2):217-21. Chin Med J (Engl). 2002. PMID: 11940335

3

[Neonatal screening for congenital adrenal hyperplasia in Shanghai areas].

Gu X, Zhou J, Ye J. Gu X, et al. Zhonghua Yu Fang Yi Xue Za Zhi. 2002 Jan;36(1):16-8. Zhonghua Yu Fang Yi Xue Za Zhi. 2002. PMID: 11955341 Chinese.

4

[Expression of green fluorescent protein vector by promoter sequence of CYP21 gene and CYP21P gene].

Han B, Wang XM, Zhang YF, Gu XF. Han B, et al. Among authors: gu xf. Yi Chuan Xue Bao. 2002 May;29(5):396-401. Yi Chuan Xue Bao. 2002. PMID: 12043565 Chinese.

5

[Technique of PCR-ACRS for the detection of CYP21 gene mutations].

Liao XY, Zhang YF, Gu XF. Liao XY, et al. Among authors: gu xf. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Oct;20(5):449-51. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14556206 Chinese.

6

[CYP21 gene point mutations study in 21-hydroxylase deficiency patients].

Liao XY, Zhang YF, Gu XF. Liao XY, et al. Among authors: gu xf. Zhonghua Er Ke Za Zhi. 2003 Sep;41(9):670-4. Zhonghua Er Ke Za Zhi. 2003. PMID: 14733808 Chinese.

7

[Genotype and phenotype correlation in Chinese patients with Wilson's Disease].

Liu XQ, Zhang YF, Liu TT, Gu XF, Hsiao KJ, Bao KR, Yu LH. Liu XQ, et al. Among authors: gu xf. Zhonghua Er Ke Za Zhi. 2003 Jan;41(1):35-8. Zhonghua Er Ke Za Zhi. 2003. PMID: 14761325 Chinese.

8

Correlation of ATP7B genotype with phenotype in Chinese patients with Wilson disease.

Liu XQ, Zhang YF, Liu TT, Hsiao KJ, Zhang JM, Gu XF, Bao KR, Yu LH, Wang MX. Liu XQ, et al. Among authors: gu xf. World J Gastroenterol. 2004 Feb 15;10(4):590-3. doi: 10.3748/wjg.v10.i4.590. World J Gastroenterol. 2004. PMID: 14966923 Free PMC article.

9

[Study on mutations of exon 12 of the PAH gene in 127 phenylketonuria patients].

Qiu WJ, Zhang YF, Ye J, Han LS, Gu XF. Qiu WJ, et al. Among authors: gu xf. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):261-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192831 Chinese.

10

[A pilot study of selective screening for high risk children with inborn error of metabolism using tandem mass spectrometry in China].

Gu XF, Han LS, Gao XL, Yan YL, Ye J, Qiu WJ. Gu XF, et al. Zhonghua Er Ke Za Zhi. 2004 Jun;42(6):401-4. Zhonghua Er Ke Za Zhi. 2004. PMID: 15265419 Chinese.

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