Kim JW - Search Results

1

Overcoming challenges associated with identifying FBN1 deep intronic variants through whole-genome sequencing.

Kim JA, Jang MA, Jang SY, Kim DK, Kim YG, Kim JW, Park TK, Jang JH. Kim JA, et al. Among authors: kim dk, kim jw, kim yg. J Clin Lab Anal. 2024 Jan;38(1-2):e25009. doi: 10.1002/jcla.25009. Epub 2024 Jan 17. J Clin Lab Anal. 2024. PMID: 38234087 Free PMC article.

2

Distributions of ACE and APOE polymorphisms and their relations with dementia status in Korean centenarians.

Choi YH, Kim JH, Kim DK, Kim JW, Kim DK, Lee MS, Kim CH, Park SC. Choi YH, et al. Among authors: kim ch, kim dk, kim jw, kim jh. J Gerontol A Biol Sci Med Sci. 2003 Mar;58(3):227-31. doi: 10.1093/gerona/58.3.m227. J Gerontol A Biol Sci Med Sci. 2003. PMID: 12634288

3

Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.

Hong JS, Ki CS, Kim JW, Suh YL, Kim JS, Baek KK, Kim BJ, Ahn KJ, Kim DK. Hong JS, et al. Among authors: kim dk, kim bj, kim js, kim jw. J Korean Med Sci. 2005 Apr;20(2):283-90. doi: 10.3346/jkms.2005.20.2.283. J Korean Med Sci. 2005. PMID: 15832002 Free PMC article.

4

A novel COL3A1 gene mutation in patient with aortic dissected aneurysm and cervical artery dissections.

Lee ST, Kim JA, Jang SY, Kim DK, Kim JW, Ki CS. Lee ST, et al. Among authors: kim ja, kim dk, kim jw. Heart Vessels. 2008 Mar;23(2):144-8. doi: 10.1007/s00380-007-1027-4. Epub 2008 Apr 4. Heart Vessels. 2008. PMID: 18389341

5

Clinical features and mutations in the ENG, ACVRL1, and SMAD4 genes in Korean patients with hereditary hemorrhagic telangiectasia.

Lee ST, Kim JA, Jang SY, Kim DK, Do YS, Suh GY, Kim JW, Ki CS. Lee ST, et al. Among authors: kim ja, kim dk, kim jw. J Korean Med Sci. 2009 Feb;24(1):69-76. doi: 10.3346/jkms.2009.24.1.69. Epub 2009 Feb 28. J Korean Med Sci. 2009. PMID: 19270816 Free PMC article.

6

Clinical, pathological, and genetic analysis of a Korean family with thoracic aortic aneurysms and dissections carrying a novel Asp26Tyr mutation.

Yoo EH, Choi SH, Jang SY, Suh YL, Lee I, Song JK, Choe YH, Kim JW, Ki CS, Kim DK. Yoo EH, et al. Among authors: kim dk, kim jw. Ann Clin Lab Sci. 2010 Summer;40(3):278-84. Ann Clin Lab Sci. 2010. PMID: 20689142

7

JAK2 V617F and MPL W515L/K mutations in Korean patients with essential thrombocythemia.

Kim HJ, Jang JH, Yoo EH, Kim HJ, Ki CS, Kim JW, Kim SH. Kim HJ, et al. Among authors: kim sh, kim jw. Korean J Lab Med. 2010 Oct;30(5):474-6. doi: 10.3343/kjlm.2010.30.5.474. Korean J Lab Med. 2010. PMID: 20890078

8

Multiplex ligation-dependent probe amplification assay for diagnosis of congenital adrenal hyperplasia.

Jang JH, Jin DK, Kim JH, Tan HK, Kim JW, Lee SY, Ki CS, Park HD. Jang JH, et al. Among authors: kim jw, kim jh. Ann Clin Lab Sci. 2011 Fall;41(1):44-7. Ann Clin Lab Sci. 2011. PMID: 21325254

9

Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing.

Jang JH, Lee JE, Kwon MJ, Ki CS, Kim JW, Nam SJ, Yang JH. Jang JH, et al. Among authors: kim jw. J Hum Genet. 2012 Mar;57(3):212-5. doi: 10.1038/jhg.2011.139. Epub 2012 Jan 5. J Hum Genet. 2012. PMID: 22217648

10

Novel mutations in CEBPA in Korean Patients with acute myeloid leukemia with a normal karyotype.

Kim S, Kim DH, Jang JH, Jung CW, Jang MA, Ki CS, Kim JW, Kim SH, Kim HJ. Kim S, et al. Among authors: kim hj, kim dh, kim sh, kim jw. Ann Lab Med. 2012 Mar;32(2):153-7. doi: 10.3343/alm.2012.32.2.153. Epub 2012 Feb 23. Ann Lab Med. 2012. PMID: 22389883 Free PMC article.

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