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1 Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis
Ali Al Ahmari, Osama Alsmadi, Atia Sheereen, Tanziel Elamin, Amal Jabr, Lina El-Baik, Safa Alhissi, Bandar Al Saud, Moheeb Al-Awwami, Ibrahim Al Fawaz, Mouhab Ayas, Khawar Siddiqui, Abbas Hawwari
Blood Res.2021;56(2):86-101.   Published online 2021 June 30     DOI: http://dx.doi.org/10.5045/br.2021.2020308
      
2 Prostate Cancer in a Patient with a Family History of BRCA Mutation: a Case Report and Literature Review
Won Hoon Song, Sung Han Kim, Jae Young Joung, Weon Seo Park, Ho Kyung Seo, Jinsoo Chung, Kang Hyun Lee
J Korean Med Sci.2017;32(2):377-381.   Published online 2016 December 7     DOI: http://dx.doi.org/10.3346/jkms.2017.32.2.377
      
3 Biochemical and Genetic Analysis of Seven Korean Individuals With Suspected Metachromatic Leukodystrophy
Minje Han, Sun-Hee Jun, Yun-Jin Lee, Baik-Lin Eun, Seung Jun Lee, Moon-Woo Seong, Sung Sup Park, Sang Hoon Song, Hyung-Doo Park, Junghan Song
Ann Lab Med.2015;35(4):458-462.   Published online 2015 May 21     DOI: http://dx.doi.org/10.3343/alm.2015.35.4.458
      
4 A Case of Crigler-Najjar Syndrome Type 2 Diagnosed Using Genetic Mutation Analysis
Sang Yee Kim, Soo Hyun Lee, Hong Koh, Seung Tae Lee, Chang Seok Ki, Jong Won Kim, Ki Sup Chung
Korean J Pediatr Gastroenterol Nutr.2008;11(2):219-222.   Published online 2008 September 30     DOI: http://dx.doi.org/10.5223/kjpgn.2008.11.2.219
      

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