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Cited by in F6Publishing
For: Topaloğlu H. Neuromuscular disorders in Anatolia – A personal review. Neuromuscular Disorders 2019;29:152-156. [DOI: 10.1016/j.nmd.2018.12.014] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
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1 Çavdarlı B, Köken ÖY, Satılmış SBA, Bilen Ş, Ardıçlı D, Ceylan AC, Gündüz CNS, Topaloğlu H. High diagnostic yield of targeted next-generation sequencing panel as a first-tier molecular test for the patients with myopathy or muscular dystrophy. Ann Hum Genet 2022. [PMID: 36575883 DOI: 10.1111/ahg.12492] [Reference Citation Analysis]
2 Çavdarli B, Köken Ö, Ceylan AC, Semerci CN, Topaloğlu H. Genetic Landscape of Dystrofin Gene Deletions and Duplications From Turkey: A Single Center Experience. Turkish Journal of Pediatric Disease 2021. [DOI: 10.12956/tchd.913588] [Reference Citation Analysis]
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