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Jump to: 2021 | 2017 | 2016
Number of items: 3.

2021

Daimagueler, Huelya-Sevcan, Akpulat, Ugur, Oezdemir, Oezkan, Yis, Uluc, Gungor, Serdal, Talim, Beril, Diniz, Gulden, Baydan, Figen, Thiele, Holger, Altmueller, Janine, Nuernberg, Peter and Cirak, Sebahattin (2021). Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey. Am. J. Med. Genet. A, 185 (6). S. 1678 - 1691. HOBOKEN: WILEY. ISSN 1552-4833

2017

Yis, Uluc, Dixit, Vishal, Isikay, Sedat, Karakaya, Mert, Baydan, Figen, Diniz, Gulden, Polat, Ipek, Hiz-Kurul, Semra and Cirak, Sebahattin (2017). Occipital cortex dysgenesis with white matter changes due to mutations in Laminin alpha 2. Turk. J. Pediatr., 59 (3). S. 338 - 342. ANKARA: TURKISH J PEDIATRICS. ISSN 0041-4301

2016

Yis, Uluc, Baydan, Figen, Karakaya, Mert, Kurul, Semra Hiz and Cirak, Sebahattin (2016). Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies. Biomed Res. Int., 2016. LONDON: HINDAWI LTD. ISSN 2314-6141

This list was generated on Thu May 2 03:56:20 2024 CEST.