Aromatase deficiency, a rare syndrome: case report by Baykan, Emine Kartal, Erdoğan, Mehmet, Özen, Samim, Darcan, Şükran, Saygılı, L Füsun

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A Young Diabetic Case with Bloom Syndrome by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Erdogan, Mehmet, Çetinkalp, Sevki, Çogulu, Özgür, Özgen, A Gökhan, Saygili, L Füsun

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A Case of Polyglandular Autoimmune Syndrome Type One with Hypercalcemia and Hypotension by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Yaman, Miray, Erdogan, Mehmet, Çetinkalp, Sevki, Saygili, L Füsun, Darcan, Sükran, Özgen, A Gökhan

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Heterozygous AGPAT2 Mutation, Diabetes, and Lipodystrophy in Extremities by Simsir, Ilgin Yildirim, Akinci, Baris, Onay, Hüseyin, Erdogan, Mehmet, Çetinkalp, Sevki, Özgen, A Gökhan, Yilmaz, Candeger, Saygili, L Füsun

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Multiple Endocrine Neoplasia Type 4 (MEN4) Syndrome by Simsir, Ilgin Yildirim, Ertan, Yesim, Sözbilen, Murat, Makay, Özer, Erdogan, Mehmet, Çetinkalp, Sevki, Saygili, L Füsun, Yilmaz, Candeger, Berdeli, Afig, Özgen, A Gökhan

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Features of Nine Adult Cases of Osteogenesis Imperfecta by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Keklik, Fatma, Altun, Ilker, Erdogan, Mehmet, Çetinkalp, Sevki, Özgen, A Gökhan, Göksen, Damla, Saygili, L Füsun

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Magnetic Resonance Imaging Characteristics of a Dunnigan-Type Familial Partial Lipodystrophy Patient by Kutbay, Nilufer Özdemir, Yürekli, Banu Sarer, Karaca, Emin, Onay, Hüseyin, Akinci, Baris, Erdogan, Mehmet, Çetinkalp, Sevki, Seçil, Mustafa, Özgen, A Gökhan, Saygili, L Füsun

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A Case of Dyskeratosis Congenita Associated with Hypothyroidism and Hypogonadism by Kutbay, Nilüfer Özdemir, Erdemir, Zehra, Yürekli, Banu Sarer, Karaca, Emin, Erdogan, Mehmet, Çetinkalp, Sevki, Kandiloglu, Gülsen, Özgen, A Gökhan, Özkinay, Ferda, Saygili, L Füsun

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Melanocortin-4 Receptor Mutation and Obesity by Simsir, Ilgin Yildirim, Özen, Samim, Onay, Hüseyin, Erdogan, Mehmet, Göksen, Damla, Özgen, A Gökhan, Saygili, L Füsun, Darcan, Sükran, Yilmaz, Candeger, Çetinkalp, Sevki

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A Novel Mutation in Deficiency of 11 B-Hydroxylase: A Possible Association with Disease Severity by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Simsir, Ilgin Yildirim, Baykan, Emine Kartal, Kocabas, Gökçen Ünal, Onay, Hüseyin, Erdogan, Mehmet, Çetinkalp, Sevki, Özgen, AGökhan, Saygili, L Füsun

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Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome by Yürekli, Banu Sarer, Kutbay, Nilüfer Özdemir, Karaca, Emin, Erdogan, Mehmet, Çetinkalp, Sevki, Kitis, Ömer, Özgen, A Gökhan, Özkinay, Ferda, Saygili, L Füsun

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Aromatase Deficiency, a Rare Syndrome: Case Report by Pignatti, Elisa, Simoni, Manuela, Rochira, Vincenzo

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