A Novel Coincidence: Essential Thrombocythemia with Facioscapulohumeral Muscular Dystrophy by Ceren Hangül, Orhan Kemal Yücel, Aslı Toylu, Hilmi Uysal, Sibel Berker Karaüzüm

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Celiac disease in patients with Williams-Beuren syndrome by Ercan Mıhçı, Banu Güzel Nur, Sibel Berker-Karaüzüm, Aygen Yılmaz, Reha Artan

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Previously Unreported Chromosomal Aberrations of t(3;3)(q29;q23), t(4;11)(q21;q23), and t(11;18)(q10;q10) in a Patient with Accelerated Phase Ph+ CML by Cigdem Aydin, Zafer Cetin, Ozan Salim, Orhan Kemal Yucel, Levent Undar, Sibel Berker Karauzum

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Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies by Ercan Mihçi, Mualla Ozcan, Sibel Berker-Karaüzüm, Ibrahim Keser, Sükran Taçoy, Senay Hapsolat, Güven Lüleci

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The ratios of estradiol and progesterone to testosterone influence the severity of facioscapulohumeral muscular dystrophy by Ceren Hangul, Selen Bozkurt, Ugur Bilge, Sebahat Ozdem, Hasan Altunbas, Hilmi Uysal, Filiz Koc, Sibel Berker Karauzum

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Analysis of DUX4 Expression in Bone Marrow and Re-Discussion of DUX4 Function in the Health and Disease by Ceren HANGUL, Oznur TOKTA, Sibel BERKER KARAUZUM, Bahar AKKAYA, Hulya YILDIRIM, Funda TAYFUN KUPESIZ, Ayse Nur AKINEL

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