3 results  1 of 1 

1 Primary Myelofibrosis with MPL S505N Mutation: The First Case Reported in Korea
Ung-Jun Kim, Ho-Jong Lee, In-Sun Choi, Seong-Ho Kang, Sook-Jin Jang, Dae-Soo Moon, Geon Park
Lab Med Online.2018;8(4):167-170.   Published online 2018 September 28     DOI: http://dx.doi.org/10.3343/lmo.2018.8.4.167
      
2 A Rare Case of a de novo Proximal Deletion of 13q in a Neonate with Congenital Megacolon
Jae-Lim Choi, Bo-Ram Kim, Ji-Eun Kim, Kwang-Sook Woo, Kyeoung-Hee Kim, Jeong-Man Kim, Jin-A Jeong, Jin-Yeong Han
Lab Med Online.2013;3(2):119-123.   Published online 2013 April 1     DOI: http://dx.doi.org/10.3343/lmo.2013.3.2.119
      
3 A Case of Nonsyndromic Intrahepatic Bile Duct Paucity with Congenital Bilateral Vocal Cord Paralysis and 13q Deletion
Ju Young Chung, Jeong Soo Lee, Byung Eoi Kim, Myung Jai Choi, Dong Chul Park, Sang Woo Kim, Kyung Hoon Kang
Korean J Pediatr Gastroenterol Nutr.2001;4(1):108-112.   Published online 2001 April 30     DOI: http://dx.doi.org/10.5223/kjpgn.2001.4.1.108
      

 1 of 1