Lee HH - Search Results

1

Use of TaqI digestion may lead to incorrect molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Lee HH, de Wijs IJ, Sistermans EA. Lee HH, et al. Mol Genet Metab. 2000 Aug;70(4):322-4. doi: 10.1006/mgme.2000.3023. Mol Genet Metab. 2000. PMID: 10993720

2

Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency.

Lee HH, Chang SF, Lo FS, Chao HT, Lin CY. Lee HH, et al. Mol Genet Metab. 2003 Jul;79(3):214-20. doi: 10.1016/s1096-7192(03)00087-8. Mol Genet Metab. 2003. PMID: 12855227

3

Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.

Lee HH, Lee YJ, Wang YM, Chao HT, Niu DM, Chao MC, Tsai FJ, Lo FS, Lin SJ. Lee HH, et al. Among authors: lee yj. Mol Genet Metab. 2008 Apr;93(4):450-7. doi: 10.1016/j.ymgme.2007.10.008. Epub 2007 Nov 26. Mol Genet Metab. 2008. PMID: 18039588

4

Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese.

Lee HH, Kuo JM, Chao HT, Lee YJ, Chang JG, Tsai CH, Chung BC. Lee HH, et al. Among authors: lee yj. J Clin Endocrinol Metab. 2000 Feb;85(2):597-600. doi: 10.1210/jcem.85.2.6367. J Clin Endocrinol Metab. 2000. PMID: 10690861

5

CYP21 mutations and congenital adrenal hyperplasia.

Lee HH. Lee HH. Clin Genet. 2001 May;59(5):293-301. doi: 10.1034/j.1399-0004.2001.590501.x. Clin Genet. 2001. PMID: 11359457 Review.

6

Diversity of the CYP21A2 gene: a 6.2-kb TaqI fragment and a 3.2-kb TaqI fragment mistaken as CYP21A1P.

Lee HH, Tsai FJ, Lee YJ, Yang YC. Lee HH, et al. Among authors: lee yj. Mol Genet Metab. 2006 Aug;88(4):372-7. doi: 10.1016/j.ymgme.2006.03.013. Epub 2006 May 8. Mol Genet Metab. 2006. PMID: 16684614

7

Structural analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency.

Lee HH, Niu DM, Lin RW, Chan P, Lin CY. Lee HH, et al. J Hum Genet. 2002;47(10):517-22. doi: 10.1007/s100380200077. J Hum Genet. 2002. PMID: 12376740

8

The chimeric CYP21P/CYP21 gene and 21-hydroxylase deficiency.

Lee HH. Lee HH. J Hum Genet. 2004;49(2):65-72. doi: 10.1007/s10038-003-0115-2. Epub 2004 Jan 17. J Hum Genet. 2004. PMID: 14730433 Review.

9

Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module.

Lee HH. Lee HH. Mol Genet Metab. 2005 Jan;84(1):4-8. doi: 10.1016/j.ymgme.2004.09.009. Epub 2004 Nov 11. Mol Genet Metab. 2005. PMID: 15639189 Review.

10

Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia.

Lee HH, Chao HT, Ng HT, Choo KB. Lee HH, et al. J Med Genet. 1996 May;33(5):371-5. doi: 10.1136/jmg.33.5.371. J Med Genet. 1996. PMID: 8733045 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,552 results

Search Page

Filters