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Rapid detection of duplication/deletion of the PMP22 gene in patients with Charcot-Marie-Tooth disease Type 1A and hereditary neuropathy with liability to pressure palsy by real-time quantitative PCR using SYBR Green I dye.
Kim SW, Lee KS, Jin HS, Lee TM, Koo SK, Lee YJ, Jung SC. Kim SW, et al. Among authors: lee tm, lee ks, lee yj. J Korean Med Sci. 2003 Oct;18(5):727-32. doi: 10.3346/jkms.2003.18.5.727. J Korean Med Sci. 2003. PMID: 14555828 Free PMC article.
The molecular basis of phenylketonuria in Koreans.
Lee DH, Koo SK, Lee KS, Yeon YJ, Oh HJ, Kim SW, Lee SJ, Kim SS, Lee JE, Jo I, Jung SC. Lee DH, et al. Among authors: lee sj, lee ks, lee je. J Hum Genet. 2004;49(11):617-621. doi: 10.1007/s10038-004-0197-5. Epub 2004 Oct 16. J Hum Genet. 2004. PMID: 15503242
Mesomelic dwarfism in pseudoachondroplasia.
Song HR, Li QW, Oh CW, Lee KS, Koo SK, Jung SC. Song HR, et al. Among authors: lee ks. J Pediatr Orthop B. 2004 Sep;13(5):340-4. doi: 10.1097/01202412-200409000-00012. J Pediatr Orthop B. 2004. PMID: 15552564
6,076 results