Identification of copy number variants in children and adolescents with autism spectrum disorder: a study from Turkey von Özaslan, Ahmet, Kayhan, Gülsüm, İşeri, Elvan, Ergün, Mehmet Ali, Güney, Esra, Perçin, Ferda Emriye

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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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Diagnostic Yield of Molecular Karyotyping of Idiopathic Intellectual Disability Patients Ended with One Causative Anomaly; Duplication 9q34 Syndrome von Çavdarlı,Büşranur, Perçin,Emriye Ferda, Yirmibeş Karaoğuz,Meral, Ergün,Mehmet Ali

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The relation between isolated micropenis in childhood with CAG and GGN repeat polymorphisms in the androgen receptor gene von Tuğ, Esra, Güntekin Ergün, Sezen, Ergün, Mehmet Ali, Dilek, Fatma Nihal, Perçin, Emriye Ferda

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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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Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey von Kan Karaer, Derya, Ergün, Mehmet Ali, Ruhi, Hatice Ilgın, Öztürk, Jale, Kara, Halil, Reisoğlu Çakmak, Deniz, Aydoğmuş, Talihanur, Perçin, Emriye Ferda

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Diagnosis of the Genomic Imprinting Diseases by the Usage of Conventional and Molecular Analyses von Öztürk Kaymak,Ayşegül, Gücüyener,Kıvılcım, Yirmibeş Karaoğuz,Meral, Perçin,Emriye Ferda

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Thrombophilic Status of Extracted Fetal Tissues of Spontaneously Aborted Embroys von Erdem,Ahmet, Balabanlı,Kanuni Barbaros, Pala,Elif, Yirmibeş Karaoğuz,Meral, Perçin,Emriye Ferda

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Molecular Karyotyping in Anorectal Malformations: Could DGCR6 Gene Haploinsufficiency Cause Anal Atresia in 22q11 Deletion Syndrome? von Çubuk, Pelin Özyavuz, Kayhan, Gülsüm, Perçin, Ferda Emriye

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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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Intelligent Ratio: A New Method for Carrier and Newborn Screening in Spinal Muscular Atrophy von Cavdarli, Busranur, Ozturk, Fatma Nihal, Guntekin Ergun, Sezen, Ergun, Mehmet Ali, Dogan, Ozlem, Percin, Emriye Ferda

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Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing von Bakır, Abdullatif, Yirmibeş Karaoğuz, Meral, Perçin, Ferda Emriye, Tuğ, Esra, Cinaz, Peyami, Ergün, Mehmet Ali

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Genome-wide association and whole exome sequencing studies reveal a novel candidate locus for restless legs syndrome von Ergun, Ufuk, Say, Bahar, Ergun, Sezen Guntekin, Percin, Ferda Emriye, Inan, Levent, Kaygisiz, Sukran, Asal, Pınar Gelener, Yurteri, Buket, Struchalin, Maksim, Shtokalo, Dmitry, Ergun, Mehmet Ali

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46 XX male syndrome with hypogonadotropic hypogonadism: A case report von Yalcin, Mehmet M, Ozkan, Cigdem, Akturk, Mujde, Percin, Ferda Emriye, Altinova, Alev, Karakoc, Ayhan, Ayvaz, Goksun, Cakir, Nuri

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6.1 A STUDY FROM TURKEY: IDENTIFICATION OF COPY NUMBER VARIANTS IN CHILDREN AND ADOLESCENTS WITH AUTISM SPECTRUM DISORDER von Özaslan, Ahmet, Kayhan, Gülsüm, Işeri, Elvan, Ergün, Mehmet Ali, Güney, Esra, Emriye Perçin, Ferda

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Spondylocostal dysostosis associated with type I split cord malformation and double nipple on one side: a case report von Yilmaz, Muhammet Bahadır, Kaymak, Aysegul, Kurt, Gokhan, Percin, Ferda Emriye, Baykaner, Kemali

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Investigation of Submicroscopic Chromosomal Anomalies on Patients with Unexplained Intellectual Disabilities with Molecular Karyotyping

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Fibrillin-1 gene intron 56 polymorphism in Turkish children with mitral valve prolapse von Ozdemir, Osman, Olgunturk, Rana, Karaer, Kadri, Ergun, Mehmet Ali, Tunaoglu, Fatma Sedef, Kula, Serdar, Percin, Ferda Emriye

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Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia von Yazıcıoğlu, Burcu, Kaya, Zühre, Güntekin Ergun, Sezen, Perçin, Ferda, Koçak, Ülker, Yenicesu, İdil, Gürsel, Türkiz

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Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis von Sarıman, Melda, Abacı, Neslihan, Sırma Ekmekçi, Sema, Çakiris, Aris, Perçin Paçal, Ferda, Üstek, Duran, Ayer, Mesut, Yenerel, Mustafa Nuri, Beşışık, Sevgi, Çefle, Kıvanç, Palandüz, Şükrü, Öztürk, Şükrü

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