Clinical Evidence of Crossover in the SHOX Gene by Emine Göktaş, Mahmut Selman Yıldırım

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Familial 22q11.2 deletion syndrome with autosomal dominant inheritance by Bahar Gokturk, Mahmut Gokdemir, ismail Reisli, Mahmut Selman Yildirim

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X Chromosome Pericentric Inversion: Report of a Case with 46,X,inv(X)(p11.2q26) and a Mini-Review of the Literature by Emine Göktaş, Betül Okur Altındaş, Ayşe Gül Zamani, Mahmut Selman Yıldırım

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A case with ICF syndrome lost to rubella pneumonitis by Ismail Reisli, Mahmut Selman Yildirim, Yavuz Köksal, Mustafa Cihat Avunduk, Aynur Acar

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A Turkish Family with Loeys-dietz Syndrome and a Report of a Homozygous Patient with SMAD3 Pathogenic Variation by Betul Okur Altindas, Ayse Gul Zamani, Mehmet Burhan Oflaz, Muhammed Gunes, Mahmut Selman Yildirim

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Evaluation of immunological abnormalities in patients with rare syndromes by Yahya Gul, Hasan Kapakli, Selma Erol Aytekin, Şukru Nail Guner, Sevgi Keles, Ayşe Gül Zamani, Mahmut Selman Yildirim, Ïsmail Reisli

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ERCC1 and XRCC1 single nucleotide polymorphisms can guide treatment decision in patients with metastatic non-small cell lung cancer by Mustafa Karaagac, Mehmet Artac, Caglayan Geredeli, Melek Karakurt Eryilmaz, Mahmut Selman Yildirim, Tuba Akkuloglu, Ali Inal, Abdurrahman Isikdogan, Hakan Bozcuk, Ahmet Demirkazik

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