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Material Type: Artigo
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Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han PopulationSun, Ying ; Yuan, Yi ; Yang, Hua ; Li, Jingjie ; Feng, Tian ; Ouyang, Yongri ; Jin, Tianbo ; Liu, MingJournal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.405-410 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek PopulationÖzcabı, Bahar ; Tahmiscioğlu Bucak, Feride ; Jaferova, Sevinç ; Oruç, Çiğdem ; Adrovic, Amra ; Ceylaner, Serdar ; Ercan, Oya ; Evliyaoğlu, OlcayJournal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.484-489 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Genetics in Pituitary Short StatureUyguner, Z OyaJournal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2) [Periódico revisado por pares]Istanbul: Galenos Publishing HouseTexto completo disponível |
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Material Type: Artigo
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Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric HypercalcemiaPapadopoulou, Anna ; Gole, Evangelia ; Melachroinou, Katerina ; Meristoudis, Christos ; Siahanidou, Tania ; Papadimitriou, AnastasiosJournal of clinical research in pediatric endocrinology, 2016-09, Vol.8 (3), p.341-346 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Genetic Approach to OsteoporosisAlanay, YaseminJournal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2) [Periódico revisado por pares]Istanbul: Galenos Publishing HouseTexto completo disponível |
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Material Type: Artigo
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Screening of HHEX Mutations in Chinese Children with Thyroid DysgenesisLiu, Shiguo ; Chai, Jian ; Zheng, Guohua ; Li, Huichao ; Lu, Deguo ; Ge, YinlinJournal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.21-25 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai PatientSriphrapradang, Chutintorn ; Thewjitcharoen, Yotsapon ; Chanprasertyothin, Suwannee ; Nakasatien, Soontaree ; Himathongkam, Thep ; Trachoo, ObjoonJournal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.241-245 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) SyndromeDöneray, Hakan ; Usui, Takeshi ; Kaya, Avni ; Dönmez, Ayşe SenaJournal of clinical research in pediatric endocrinology, 2015-06, Vol.7 (2), p.140-143 [Periódico revisado por pares]Turkey: Galenos Publishing HouseTexto completo disponível |
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Material Type: Artigo
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish FamilyDursun, Fatma ; Mohamoud, Hussein Sheikh Ali ; Karim, Noreen ; Naeem, Muhammad ; Jelani, Musharraf ; Kırmızıbekmez, HevesJournal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.472-477 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Clinical and Mutational Features of Three Chinese Children with Congenital Generalized LipodystrophySu, Xueying ; Lin, Ruizhu ; Huang, Yonglan ; Sheng, Huiying ; Li, Xiaofei ; Ting, Tzer Hwu ; Liu, Li ; Li, Xiuzhen Darendeliler,Fatma FeyzaJournal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.52-57 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |