Han B - Search Results

1

[Detection of trisomy 21 by quantitative fluorescent PCR in clinical samples undergoing prenatal diagnosis for hereditary hearing loss].

Lu YP, Cheng J, Han B, Wang LX, Dai P, Yuan HJ, Li YL. Lu YP, et al. Among authors: han b. Zhonghua Fu Chan Ke Za Zhi. 2011 Jun;46(6):427-30. Zhonghua Fu Chan Ke Za Zhi. 2011. PMID: 21781583 Chinese.

2

[Genetic counseling and instruction for deaf couples directed by genetic testing].

Han B, Dai P, Wang GJ, Kang DY, Zhang X, Yuan YY, Zhu QW, Jin ZC, Li M, Zhai SQ, Huang DL, Han DY. Han B, et al. Among authors: han dy. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jul;42(7):499-503. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17886676 Chinese.

3

[Prenatal diagnosis for hereditary deaf families assisted by genetic testing].

Han B, Dai P, Qi QW, Wang LX, Wang Y, Bian XM, Wang QJ, Zhang X, Kang DY, Wang GJ, Han DY. Han B, et al. Among authors: han dy. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Sep;42(9):660-3. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18051563 Chinese.

4

[Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].

Li Q, Dai P, Huang DL, Yuan YY, Zhu QW, Han B, Liu X, Yu F, Kang DY, Zhang X, Xue DD, Jin ZC. Li Q, et al. Among authors: han b. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Dec;42(12):893-7. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18335745 Chinese.

5

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.

Dai P, Li Q, Huang D, Yuan Y, Kang D, Miller DT, Shao H, Zhu Q, He J, Yu F, Liu X, Han B, Yuan H, Platt OS, Han D, Wu BL. Dai P, et al. Among authors: han b, han d. Genet Med. 2008 Aug;10(8):586-92. doi: 10.1097/gim.0b013e31817d2ef1. Genet Med. 2008. PMID: 18641518

6

Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairment.

Han B, Cheng J, Yang SZ, Cao JY, Shen WD, Ji F, Kang DY, Zhang X, Dai P, Yuan HJ. Han B, et al. Chin Med J (Engl). 2009 Apr 5;122(7):830-3. Chin Med J (Engl). 2009. PMID: 19493398

7

[Development of multiple quantitative fluorescent PCR for rapid diagnosis of common aneuploidy and it's clinical application].

Lu YP, Cheng J, Jiang SF, Zhang LW, Gao ZY, Han B, Yuan HJ, Li YL. Lu YP, et al. Among authors: han b. Yi Chuan. 2010 Nov;32(11):1141-6. Yi Chuan. 2010. PMID: 21513165 Chinese.

8

[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China].

Dai P, Yu F, Han B, Wu H, Yuan YY, Li Q, Wang GJ, Liu X, He J, Huang DL, Kang DY, Zhang X, Yuan HJ, Leejun CW, Han DY. Dai P, et al. Among authors: han b, han dy. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Nov;42(11):804-8. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18300439 Chinese.

9

[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].

Dai P, Han B, Yuan YY, Jin ZC, Wang Y, Xiang Y, Yu F, Liu X, Wang GJ, Kang DY, Zhang X, Li M, Zhai SQ, Huang DL, Han DY. Dai P, et al. Among authors: han b, han dy. Zhonghua Yi Xue Za Zhi. 2007 Apr 24;87(16):1088-92. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17672986 Chinese.

10

[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2].

Chen J, Yang SZ, Liu J, Han B, Wang GJ, Zhang X, Kang DY, Dai P, Young WY, Yuan HJ. Chen J, et al. Among authors: han b. Yi Chuan. 2008 Apr;30(4):433-8. doi: 10.3724/sp.j.1005.2008.00433. Yi Chuan. 2008. PMID: 18424413 Chinese.

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