He L - Search Results

1

A novel insertion mutation in spastin gene is the cause of spastic paraplegia in a Chinese family.

Qin W, Zhang T, Han J, Tang L, Li X, Feng G, Liu W, He L. Qin W, et al. Among authors: he l. J Neurol Sci. 2003 Jun 15;210(1-2):35-9. doi: 10.1016/s0022-510x(03)00011-x. J Neurol Sci. 2003. PMID: 12736085

2

Polymorphisms of chromogranin B gene associated with schizophrenia in Chinese Han population.

Zhang B, Tan Z, Zhang C, Shi Y, Lin Z, Gu N, Feng G, He L. Zhang B, et al. Among authors: he l. Neurosci Lett. 2002 May 3;323(3):229-33. doi: 10.1016/s0304-3940(02)00145-3. Neurosci Lett. 2002. PMID: 11959426

3

[Allelic analysis on chromosome 5 in sporadic colorectal cancer patients].

Zhang F, Zhou C, Ling Y, Qiu G, Bai S, Liu W, He L, Peng Z. Zhang F, et al. Among authors: he l. Zhonghua Zhong Liu Za Zhi. 2002 Sep;24(5):458-60. Zhonghua Zhong Liu Za Zhi. 2002. PMID: 12485498 Chinese.

4

[Loss of heterozygosity analysis to define putative region involved in tumor differentiation and metastases in sporadic colorectal cancer patients].

Peng Z, Zhang F, Zhou C, Qiu G, Bai S, Liu W, He L. Peng Z, et al. Among authors: he l. Zhonghua Wai Ke Za Zhi. 2002 Oct;40(10):776-9. Zhonghua Wai Ke Za Zhi. 2002. PMID: 12487884 Chinese.

5

Loss of heterozygosity of chromosome 20 in sporadic colorectal cancer.

Peng Z, Zhou C, Zhang F, Ling Y, Tang H, Bai S, Liu W, Qiu G, He L. Peng Z, et al. Among authors: he l. Chin Med J (Engl). 2002 Oct;115(10):1529-32. Chin Med J (Engl). 2002. PMID: 12490103

6

A locus for congenital preauricular fistula maps to chromosome 8q11.1-q13.3.

Zou F, Peng Y, Wang X, Sun A, Liu W, Bai S, Zhu H, Gao B, Feng G, He L. Zou F, et al. Among authors: he l. J Hum Genet. 2003;48(3):155-8. doi: 10.1007/s100380300024. J Hum Genet. 2003. PMID: 12624728

7

A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

Xing QH, Wang MT, Chen XD, Feng GY, Ji HY, Yang JD, Gao JJ, Qin W, Qian XQ, Wu SN, He L. Xing QH, et al. Among authors: he l. Am J Hum Genet. 2003 Aug;73(2):377-82. doi: 10.1086/377007. Epub 2003 Jun 12. Am J Hum Genet. 2003. PMID: 12815562 Free PMC article.

8

Association of APOE gene with schizophrenia in Chinese: a possible risk factor in times of malnutrition.

Liu W, Breen G, Zhang J, Li S, Gu N, Feng G, Bai S, Shen T, Yu A, Xue H, St Clair D, He L. Liu W, et al. Among authors: he l. Schizophr Res. 2003 Aug 1;62(3):225-30. doi: 10.1016/s0920-9964(02)00384-5. Schizophr Res. 2003. PMID: 12837518

9

Evidence for a major susceptibility locus at 11q22.1-23.3 has been detected in a large Chinese family with pure grand mal epilepsy.

Yang MS, Wang XF, Qin W, Feng GY, He L. Yang MS, et al. Among authors: he l. Neurosci Lett. 2003 Aug 7;346(3):133-6. doi: 10.1016/s0304-3940(03)00500-7. Neurosci Lett. 2003. PMID: 12853102

10

[Transmission disequilibrium test of polymorphisms of serotonin transporter gene and schizophrenia based on family trios].

Sun WW, Fan JB, Qian XQ, Tang JX, Xing YL, Shi JG, Zhu SM, Liu HJ, Gu NF, Feng GY, He L. Sun WW, et al. Among authors: he l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):342-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12903048 Chinese.

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