Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease by Jolly, Angad, Bayram, Yavuz, Turan, Serap, Aycan, Zehra, Tos, Tulay, Abali, Zehra Yavas, Hacihamdioglu, Bulent, Coban Akdemir, Zeynep Hande, Hijazi, Hadia, Bas, Serpil, Atay, Zeynep, Guran, Tulay, Abali, Saygin, Bas, Firdevs, Darendeliler, Feyza, Colombo, Roberto, Barakat, Tahsin Stefan, Rinne, Tuula, White, Janson J, Yesil, Gozde, Gezdirici, Alper, Gulec, Elif Yilmaz, Karaca, Ender, Pehlivan, Davut, Jhangiani, Shalini N, Muzny, Donna M, Poyrazoglu, Sukran, Bereket, Abdullah, Gibbs, Richard A, Posey, Jennifer E, Lupski, James R

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Preterm ovarian hyperstimulation syndrome mimicking clitoromegaly by Ay, Zeynep Alize, Abali, Saygin, Korkmaz, Ayse, Beken, Serdar

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Early postnatal metabolic profile in neonates with critical CHDs by Guvenc, Osman, Beken, Serdar, Abali, Saygin, Saral, Neslihan Yildirim, Yalcin, Gizem, Albayrak, Eda, Bulum, Burcu, Demirelce, Ozlem, Basgoze, Serdar, Odemis, Ender, Erek, Ersin, Serteser, Mustafa, Toygar, Ayse Korkmaz

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Neonatal Problems and Infancy Growth of Term SGA Infants: Does “SGA” Definition Need to Be Re-evaluated? by Abali, Saygin, Beken, Serdar, Albayrak, Eda, Inamlik, Aysegul, Bulum, Burcu, Bulbul, Ezgi, Eksi, Gulten Zeynep, Ay, Zeynep Alize, Karabay, Melis, Kaya, Didem, Halici, Muge, Semiz, Serap, Korkmaz, Ayse

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Early Postnatal Metabolic Profile in Neonates With Different Birth Weight Status: A Pilot Study by Beken, Serdar, Abali, Saygin, Yildirim Saral, Neslihan, Guner, Bengisu, Dinc, Taha, Albayrak, Eda, Ersoy, Melike, Kilercik, Meltem, Halici, Muge, Bulbul, Ezgi, Kaya, Didem, Karabay, Melis, Ay, Zeynep Alize, Eksi, Gulten Zeynep, Benli Aksungar, Fehime, Korkmaz, Ayse, Serteser, Mustafa

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CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation by Karti, Omer, Abali, Saygin, Ayhan, Ziya, Gokmeydan, Eylem, Nalcaci, Serhad, Yaman, Aylin, Saatci, Ali Osman

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Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features by Eltan, Mehmet, Yavas Abali, Zehra, Turkyilmaz, Ayberk, Gokce, Ibrahim, Abali, Saygın, Alavanda, Ceren, Arman, Ahmet, Kirkgoz, Tarik, Guran, Tulay, Hatun, Sukru, Bereket, Abdullah, Turan, Serap

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The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography by Karti, Omer, Nalbantoglu, Ozlem, Abali, Saygin, Tunc, Selma, Ozkan, Behzat

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Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS by Turan, Serap, Thiele, Susanne, Tafaj, Olta, Brix, Bettina, Atay, Zeynep, Abali, Saygin, Haliloglu, Belma, Bereket, Abdullah, Bastepe, Murat

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Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis by Kühnen, Peter, Turan, Serap, Fröhler, Sebastian, Güran, Tülay, Abali, Saygin, Biebermann, Heike, Bereket, Abdullah, Grüters, Annette, Chen, Wei, Krude, Heiko

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Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia by Haliloglu, Belma, Guran, Tulay, Atay, Zeynep, Abali, Saygın, Mornet, Etienne, Bereket, Abdullah, Turan, Serap

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Comparison of two different GnRH analogs' impact on final height in girls with early puberty: Triptorelin acetate vs. leuprolide acetate by Aka, S, Abali, S, Taskin, A, Bengur, F B, Semiz, S

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Novel homozygous inactivating mutation of the calcium-sensing receptor gene ( CASR ) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet by Atay, Zeynep, Bereket, Abdullah, Haliloglu, Belma, Abali, Saygin, Ozdogan, Tutku, Altuncu, Emel, Canaff, Lucie, Vilaça, Tatiane, Wong, Betty Y.L, Cole, David E.C, Hendy, Geoffrey N, Turan, Serap

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Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross‐sectional study by Hatun, S., Yesiltepe Mutlu, G., Cinaz, P., Turan, S., Ekberzade, A., Bereket, A., Erbas, M. Y., Akcay, T., Onal, H., Bolu, S., Arslanoglu, I., Doger, E., Yilmaz, A. A., Ucakturk, A., Karabulut, G. S., Tuhan, H. Ü., Demir, K., Erdeve, S. S., Aycan, Z., Nalbantoğlu, Ö., Kara, C., Gungor, N.

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Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex developmentResearch in context by Chrysanthi Kouri, Grit Sommer, Idoia Martinez de Lapiscina, Rawda Naamneh Elzenaty, Lloyd J.W. Tack, Martine Cools, S. Faisal Ahmed, Christa E. Flück, Saygin Abali, Zehra Yavas Abali, Leyla Akin, Maricruz Almaraz, Laura Audí, Murat Aydin, Antonio Balsamo, Federico Baronio, Jillian Bryce, Kanetee Busiah, Maria Caimari, Núria Camats-Tarruella, Ariadna Campos-Martorell, Luis Castaño, Anna Casteràs, Semra Çetinkaya, Yee-Ming Chan, Hedi L. Claahsen-van der Grinten, Ines Costa, Fatma Feyza Darendeliler, Justin H. Davies, Isabel Esteva, Helena Fabbri-Scallet, Courtney A. Finlayson, Emilio Garcia, Beatriz Garcia Cuartero, Alina German, Evgenia Globa, Gil Guerra-Junior, Julio Guerrero, Tulay Guran, Sabine E. Hannema, Olaf Hiort, Josephine Hirsch, Leuan Hughes, Marco Janner, Zofia Kolesinska, Katherine Lachlan, Anna Lauber-Biason, Jana Krenek Malikova, Dagmar l'Allemand, Nina Lenhnerr-Taube, Angela Lucas-Herald, Jamala Mammadova, Kenneth MсElreavey, Veronica Mericq, Isabel Mönig, Francisca Moreno, Julia Mührer, Marek Niedziela, Anna Nordenstrom, Burçe Orman, Sukran Poyrazoglu, Jose M. Rial, Meilan M. Rutter, Amaia Rodríguez, Tara Schafer-Kalkhoff, Kay-Sara Sauter, Sumudu Nimali Seneviratne, Maria Sredkova-Ruskova, Rieko Tadokoro-Cuccaro, Ajay Thankamony, Mónica Tomé, Amaia Vela, Malgorzata Wasniewska, David Zangen, Nataliya Zelinska

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Premature Pubarche, Hyperinsulinemia, Hypothyroxinemia and Hyperintensities in Basal Ganglia: All Caused by a Single Congenital Defect by Bas, Serpil, Güran, Tülay, Atay, Zeynep, Haliloglu, Belma, Abali, Saygin, Turan, Serap, Bereket, Abdullah

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A Rare Presentation of Friedreich's Ataxia in Pediatric Case: Diabetes Mellitus by Bas, Serpil, Abali, Saygin, Atay, Zeynep, Gurbanov, Ziya, Çam, Sevda, Türkdogan, Dilsad, Turan, Serap, Bereket, Abdullah

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H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus by Abali, Saygin, Atay, Zeynep, Bas, Serpil, Babay, Sofia, Molho-Pessach, Vered, Zlotogorski, Abraham, Bereket, Abdullah, Turan, Serap

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Effect of iron supplementation on development of iron deficiency anemia in breastfed infants by Gokcay, Gulbin, Ozden, Tulin, Karakas, Zeynep, Karabayir, Nalan, Yildiz, Ismail, Abali, Saygin, Sahip, Yusuf

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A rare cause of hypertension in childhood: Questions by Kucuk, Nuran, Yavas Abali, Zehra, Abali, Saygın, Canpolat, Nur, Yesil, Gozde, Turan, Serap, Bereket, Abdullah, Guran, Tulay

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