Cheng K - Search Results

1

Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiency.

Zhu H, Liu W, Han B, Fan M, Zhao S, Wang H, Lu Y, Pan C, Chen F, Chen M, Song H, Cheng K, Qiao J. Zhu H, et al. Among authors: cheng k. Clin Endocrinol (Oxf). 2014 Nov;81(5):711-20. doi: 10.1111/cen.12456. Epub 2014 Apr 21. Clin Endocrinol (Oxf). 2014. PMID: 24665940

2

A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism.

Qiao J, Han B, Liu BL, Chen X, Ru Y, Cheng KX, Chen FG, Zhao SX, Liang J, Lu YL, Tang JF, Wu YX, Wu WL, Chen JL, Chen MD, Song HD. Qiao J, et al. Hum Mutat. 2009 Sep;30(9):E855-65. doi: 10.1002/humu.21072. Hum Mutat. 2009. PMID: 19551906

3

Identifying a novel mutation of CYP17A1 gene from five Chinese 17α-hydroxylase/17, 20-lyase deficiency patients.

Han B, Liu W, Zuo CL, Zhu H, Li L, Xu C, Wang XJ, Liu BL, Pan CM, Lu YL, Wu WL, Chen MD, Song HD, Cheng KX, Qiao J. Han B, et al. Gene. 2013 Mar 10;516(2):345-50. doi: 10.1016/j.gene.2012.12.010. Epub 2013 Jan 2. Gene. 2013. PMID: 23291414

4

Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effect.

Han B, Xue L, Fan M, Zhao S, Liu W, Zhu H, Cheng T, Lu Y, Cheng K, Song H, Liu Y, Qiao J. Han B, et al. Among authors: cheng k, cheng t. Endocrine. 2016 Sep;53(3):784-90. doi: 10.1007/s12020-016-0957-y. Epub 2016 May 5. Endocrine. 2016. PMID: 27150612

5

Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization.

Zhu WJ, Cheng T, Zhu H, Han B, Fan MX, Gu T, Zhao SX, Liu Y, Cheng KX, Song HD, Qiao J. Zhu WJ, et al. Mol Cell Endocrinol. 2016 Sep 15;433:66-74. doi: 10.1016/j.mce.2016.05.025. Epub 2016 May 30. Mol Cell Endocrinol. 2016. PMID: 27256151

6

A New Surgical Procedure for Penile Reconstruction by Combined Free Radial Forearm Flap and Dorsalis Pedis Flap.

Ma S, Cheng K, Liu Y, Chen F. Ma S, et al. Among authors: cheng k. Urology. 2016 Nov;97:232-237. doi: 10.1016/j.urology.2016.03.076. Epub 2016 Aug 12. Urology. 2016. PMID: 27527409

7

Author Reply.

Ma S, Cheng K, Liu Y, Chen F. Ma S, et al. Among authors: cheng k. Urology. 2016 Nov;97:237. doi: 10.1016/j.urology.2016.03.078. Epub 2016 Oct 10. Urology. 2016. PMID: 27745708 No abstract available.

8

Comment on World's First Baby Born Through Natural Insemination by Father With Total Phalloplasty Reconstruction.

Cheng K, Cheng C, Chen F, Ma S, Liu Y. Cheng K, et al. Among authors: cheng c. Ann Plast Surg. 2017 Mar;78(3):360-361. doi: 10.1097/SAP.0000000000001076. Ann Plast Surg. 2017. PMID: 28177979 No abstract available.

9

Bone morphogenetic protein 7-transduced human dermal-derived fibroblast cells differentiate into osteoblasts and form bone in vivo.

Chen F, Bi D, Cao G, Cheng C, Ma S, Liu Y, Cheng K. Chen F, et al. Among authors: cheng k, cheng c. Connect Tissue Res. 2018 May;59(3):223-232. doi: 10.1080/03008207.2017.1353085. Epub 2017 Jul 31. Connect Tissue Res. 2018. PMID: 28696808

10

Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypes.

Wang H, Zhang L, Wang N, Zhu H, Han B, Sun F, Yao H, Zhang Q, Zhu W, Cheng T, Cheng K, Liu Y, Zhao S, Song H, Qiao J. Wang H, et al. Among authors: cheng k, cheng t. Hum Genet. 2018 Mar;137(3):265-277. doi: 10.1007/s00439-018-1879-y. Epub 2018 Mar 26. Hum Genet. 2018. PMID: 29582157

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