Correction: Case presentation: a severe case of cobalamin c deficiency presenting with nephrotic syndrome, malignant hypertension and hemolytic anemia von Akar, Halil Tuna, Yıldız, Harun, Öztürk, Zeynelabidin, Karakaya, Deniz, Sezer, Abdullah, Olgaç, Asburçe

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Case report: An adolescent female with anosmic hypogonadotropic hypogonadism, intellectual disability, and papillary thyroid carcinoma: heterozygous deletion of TCF12 von Celik, Nur Berna, Sezer, Abdullah, Genel, Nebiyye, Savas-Erdeve, Senay, Karaman, İbrahim, Cetinkaya, Semra

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Case presentation: a severe case of cobalamin c deficiency presenting with nephrotic syndrome, malignant hypertension and hemolytic anemia von Akar, Halil Tuna, Yıldız, Harun, Öztürk, Zeynelabidin, Karakaya, Deniz, Sezer, Abdullah, Olgaç, Asburçe

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A founder deletion in ECM1 of 1163bp causes lipoid proteinosis in the southeast region of Turkiye von Taşdelen, Elifcan, Sezer, Abdullah, An, Isa

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DNMT3A-related overgrowth syndrome presenting with immune thrombocytopenic purpura von Sezer, Abdullah, Güneş, Öznur Kaya, Kurucu, Burçak

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A founder deletion in ECM1 of 1163 bp causes lipoid proteinosis in the southeast region of Turkiye von Taşdelen, Elifcan, Sezer, Abdullah, An, Isa

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Letter to the Editor regarding “New cases of recently described Thauvin‐Robinet‐Faivre syndrome with a novel homozygous FIBP gene variant” by Kılıç and Koşukçu, “An investigation o... von Duzenli, Tarik, Sezer, Abdullah, Percin, Ferda Emriye

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Two remarkable cases of haploinsufficiency found in the DYRK1A gene von Taşdelen, Elifcan, Tekbaş, Umut Can, Baş, Hasan, Sezer, Abdullah

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Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder von Sezer, Abdullah, Kayhan, Gulsum, Percin, Ferda E.

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Atypical presentation of ACCES syndrome resembling dominant Spondyloepiphyseal dysplasia tarda von Sezer, Abdullah, Özdemir, Zeynep, Özkan, Erdem, Çetinkaya, Semra

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Seçme Hakkının Yaş Bakımından Sınırlanması ve Osmanlı-Türkiye Anayasacılığındaki Evrimi von SEZER, Abdullah

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RMND1 Mutation Case Report and Literature Review von Bayrak, Harun, Sezer, Abdullah, Kılıç, Mustafa

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Expanding the phenotype and genotype in Thauvin‐Robinet‐Faivre syndrome: A new patient with a novel variant and additional clinical findings von Duzenli, Tarik, Sezer, Abdullah, Kayhan, Gulsum, Arslan, Ayse Tana, Percin, Ferda E.

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A homozygous missense variant in the WRN gene segregating in a family with progressive pulmonary failure with recurrent spontaneous pneumothorax and interstitial lung disease von Sezer, Abdullah, Kayhan, Gulsum, Gursoy, Tugba Ramasli, Eyuboglu, Tugba Sismanlar, Percin, Ferda E.

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A de novo heterozygous HOXA11 variant in a patient with mesomelic dysplasia with urogenital abnormalities von Sezer, Abdullah, Perçin, Ferda Emriye, Kazan, Hasan Huseyin, Kayhan, Gulsum, Akturk, Mujde

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Hypopigmented patches in Roberts/SC phocomelia syndrome occur via aneuploidy susceptibility von Sezer, Abdullah, Kayhan, Gulsum, Zenker, Martin, Percin, Emriye Ferda

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A Recurrent c.416C>T Variant in the B3GAT3 Gene in the Turkish Population: Report of Two Siblings and Expanding the Clinical Spectrum von Daşar, Tuğba, Kolkıran, Abdulkerim, Sezer, Abdullah, Bal, Ercan, Kılıç, Esra

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Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemia von Distelmaier, Felix, Sezer, Abdullah, Helm, Christina, Waldmüller, Stephan, Seibt, Annette, Gangfuß, Andrea, Kölbel, Heike, Schara-Schmidt, Ulrike, Yuksel, Deniz, Talim, Beril, Mayatepek, Ertan, Nikolin, Stefan, Weis, Joachim, Roos, Andreas, Haack, Tobias B

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15‐LOX‐1 has diverse roles in the resensitization of resistant cancer cell lines to doxorubicin von Kazan, Hasan Huseyin, Urfali‐Mamatoglu, Cagri, Yalcin, Gizem Damla, Bulut, Onur, Sezer, Abdullah, Banerjee, Sreeparna, Gunduz, Ufuk

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SERAC1 gene mutation presented with markedly alpha fetoprotein elevation: case report von Bayrak, Harun, Sezer, Abdullah, Danış, Ayşegül, Özhan, Selen Has, Yıldız, Harun, Kılıç, Mustafa

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