Huang YF - Search Results

1

A novel insertion mutation in the SEDL gene results in X-linked spondyloepiphyseal dysplasia tarda in a large Chinese pedigree.

Xia XY, Cui YX, Zhou YC, Zhou X, Shi YC, Wei L, Li XJ, Huang YF, Huang TT. Xia XY, et al. Among authors: huang tt, huang yf. Clin Chim Acta. 2009 Dec;410(1-2):39-42. doi: 10.1016/j.cca.2009.09.016. Epub 2009 Sep 19. Clin Chim Acta. 2009. PMID: 19766614

2

A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.

Wang H, Hou Y, Cui Y, Huang Y, Shi Y, Xia X, Lu H, Wang Y, Li X. Wang H, et al. Mutat Res. 2009 Mar 9;662(1-2):22-7. doi: 10.1016/j.mrfmmm.2008.11.019. Epub 2008 Dec 6. Mutat Res. 2009. PMID: 19103209

3

Molecular prenatal diagnosis in 2 pregnancies at risk for spondyloepiphyseal dysplasia congenita.

Xia XY, Cui YX, Huang YF, Pan LJ, Feng Y, Yang B, Li XJ, Zhu PY, Shi YC, Liang Q. Xia XY, et al. Among authors: huang yf. Clin Chim Acta. 2008 Jan;387(1-2):153-7. doi: 10.1016/j.cca.2007.09.006. Epub 2007 Sep 18. Clin Chim Acta. 2008. PMID: 17920052

4

A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family.

Xia XY, Cui YX, Huang YF, Pan LJ, Yang B, Wang HY, Li XJ, Shi YC, Lu HY, Zhou YC. Xia XY, et al. Among authors: huang yf. Clin Chim Acta. 2008 Dec;398(1-2):148-51. doi: 10.1016/j.cca.2008.07.030. Epub 2008 Aug 5. Clin Chim Acta. 2008. PMID: 18755172

5

Rapid molecular prenatal diagnosis of spondyloepiphyseal dysplasia congenita by PCR-SSP assay.

Cui YX, Xia XY, Bu Y, Zhou GH, Yang B, Lu HY, Shi YC, Pan LJ, Huang YF, Li XJ. Cui YX, et al. Among authors: huang yf. Genet Test. 2008 Dec;12(4):533-6. doi: 10.1089/gte.2008.0037. Genet Test. 2008. PMID: 19072565

6

Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men.

Shi YC, Wei L, Cui YX, Shang XJ, Wang HY, Xia XY, Zhou YC, Li H, Jiang HT, Zhu WM, Huang YF. Shi YC, et al. Among authors: huang yf. Clin Chim Acta. 2011 Mar 18;412(7-8):545-9. doi: 10.1016/j.cca.2010.12.005. Epub 2010 Dec 10. Clin Chim Acta. 2011. PMID: 21147082

7

A first familial G504S mutation of COL2A1 gene results in distinctive spondyloepiphyseal dysplasia congenita.

Xia X, Cui Y, Huang Y, Pan L, Wu Y, Zhang P, Jin B. Xia X, et al. Clin Chim Acta. 2007 Jul;382(1-2):148-50. doi: 10.1016/j.cca.2007.04.005. Epub 2007 Apr 14. Clin Chim Acta. 2007. PMID: 17509551 No abstract available.

8

A case of agonadism associated with y-chromosome rearrangement: cytogenetic and molecular studies.

Cui YX, Shi YC, Liu Q, Xia XY, Lu HY, Shao HF, Jia L, Yao B, Ge YF, Li XJ, Huang YF. Cui YX, et al. Among authors: huang yf. J Androl. 2009 Nov-Dec;30(6):650-4. doi: 10.2164/jandrol.108.006353. Epub 2009 Jul 17. J Androl. 2009. PMID: 19617372 Free article.

9

A G560S mutation in alpha1 (I) collagen causes familial osteogenesis imperfecta type IV.

Cui YX, Xia XY, Shi YC, Wei L, Liang Q, Yao B, Ge YF, Huang YF, Li XJ. Cui YX, et al. Among authors: huang yf. Clin Chim Acta. 2009 Nov;409(1-2):145-6. doi: 10.1016/j.cca.2009.09.008. Epub 2009 Sep 12. Clin Chim Acta. 2009. PMID: 19751715 No abstract available.

10

A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21-12p12.2 by oligonucleotide array CGH.

Lu HY, Cui YX, Shi YC, Xia XY, Liang Q, Yao B, Ge YF, Li XJ, Huang YF. Lu HY, et al. Among authors: huang yf. Am J Med Genet A. 2009 Oct;149A(10):2321-3. doi: 10.1002/ajmg.a.33030. Am J Med Genet A. 2009. PMID: 19764034 No abstract available.

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