6 results  1 of 1 

1 Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome
Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, Effat Farrokhi, Narges Abdian, Nader Bagheri, Shirin Shahbazi, Zahra Noormohammadi, Morteza Hashemzadeh Chaleshtori
Clin Exp Otorhinolaryngol.2013;6(4):201-208.   Published online 2013 November 29     DOI: http://dx.doi.org/10.3342/ceo.2013.6.4.201
      
2 A high resolution genetic mapping of the faded (fe) gene to a region between D10mit156 and D10mit193 on mouse chromosome 10
Seung-Hun Oh, Hajin Nam, Jun-Gyo Suh
Lab Anim Res.2013;29(1):33-38.   Published online 2013 March 25     DOI: http://dx.doi.org/10.5625/lar.2013.29.1.33
      
3 Mapping of the Faded (fe) Gene to a Region between D10mit191 and D10mit44 on Mouse Chromosome 10
Seung-Hun Oh, Yoonyi Nam, Jun-Gyo Suh
Lab Anim Res.2011;27(1):41-46.   Published online 2011 March 25     DOI: http://dx.doi.org/10.5625/lar.2011.27.1.41
      
4 Prenatal diagnosis of a heterozygote of salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency by genetic linkage analysis
Bo Hoon Oh, Jai Kyung Park, Yong Mook Choi, In Myung Yang, Young Seol Kim, Young Kil Choi
J Korean Med Sci.1988;3(2):73-77.   Published online 2009 May 25     DOI: http://dx.doi.org/10.3346/jkms.1988.3.2.73
      
5 The Carrier Detection and Genetic Counseling of Duchenne and Becker Muscular Dystrophy Using Linkage Analysis
Woo Nam Moon, Jae Yong Ahn, So Yeon Park, Young Cho Kim
J Korean Orthop Assoc.2000;35(3):527-532.   Published online 2000 June 30     DOI: http://dx.doi.org/10.4055/jkoa.2000.35.3.527
   
6 Screening of the Cardiac Beta Myosin Heavy Chain Gene for the Linkage to Familial Hypertrophic Cardiomyopathy in a Korean Family
Jeong-Euy Park, Cheong-Ho Lee, Hae-Kyung Kim, Jeong-Won Sohn, Gil-Hong Park, Je-Ho Lee
Korean Circ J.1994;24(6):819-833.   Published online 1994 December 31     DOI: http://dx.doi.org/10.4070/kcj.1994.24.6.819
      

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