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The Turkish Journal of Pediatrics|October 9, 1998
DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosisP Dinçer, H Topaloğlu, S AyterBrain & Development|July 1, 1993
An unusual case of Duchenne muscular dystrophyH Topaloğlu, P Dinçer, S Göğüş, et al.Brain & Development|March 1, 1996
Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patientsP Dinçer, H Topaloğlu, S Ayter, et al.Prenatal Diagnosis|January 13, 1999
Prenatal diagnosis of limb-girdle muscular dystrophy type 2CP Dinçer, F Piccolo, F Leturcq, et al.The Turkish Journal of Pediatrics|July 1, 1997
Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophyH A Taşdemir, H Topaloğlu, P Dinçer, et al.Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|July 1, 1996
Functional significance of dystrophin-positive fibers in Duchenne and Becker muscular dystrophyH A Taşdemir, E Kotiloğlu, H Topaloğlu, et al.Neuromuscular Disorders : NMD|June 6, 2000
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2FP Dinçer, C G Bönnemann, O Erdir Aker, et al.Neuropediatrics|August 1, 1997
Calpain-3 deficiency causes a mild muscular dystrophy in childhoodH Topaloğlu, P Dinçer, I Richard, et al.Journal of Medical Genetics|May 12, 2000
A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesP Dinçer, Z Akçören, E Demir, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycan gene mutations in TurkeyB Balci, E Wilichowski, G Haliloğlu, et al.Pageof 2