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European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|March 22, 2003
Frequencies of TAP1 and TAP2 gene polymorphisms in the Anatolian populationF Ozbaş-Gerçeker, M OzgüçExperimental and Molecular Pathology|January 5, 2010
Assessment of housekeeping genes for use in normalization of real time PCR in skeletal muscle with chronic degenerative changesA Yüzbaşioğlu, I Onbaşilar, C Kocaefe, et al.Brain & Development|April 17, 1999
Deletion analysis in Turkish patients with spinal muscular atrophyH Erdem, S Pehlivan, H Topaloglu, et al.The Turkish Journal of Pediatrics|January 20, 1998
Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy familiesH Erdem, S Pehlivan, H Topaloğlu, et al.Pediatric Neurology|July 3, 1998
mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girlH Topaloğlu, V Seyrantepe, N Kandemir, et al.European Journal of Pediatrics|November 1, 1994
Sodium chloride deficiency in cystic fibrosis patientsU Ozçelik, A Göçmen, N Kiper, et al.Journal of Medical Genetics|February 1, 1993
Mutation analysis in Turkish phenylketonuria patientsM Ozgüç, I Ozalp, T Coşkun, et al.The Turkish Journal of Pediatrics|January 1, 1993
Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patientsM Ozgüç, I Ozalp, T Coşkun, et al.The Turkish Journal of Pediatrics|January 1, 1993
Deletion analysis of Duchenne muscular dystrophyH Erdem, S Ayter, M Ozgüç, et al.Pediatric Hematology and Oncology|May 1, 1996
Loss of heterozygosity in the VNTR region of intron 1 of P53 in two retinoblastoma casesS Emre, A Sungur, S Bilgiç, et al.Pageof 2