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1
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population
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Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

Sun, Ying ; Yuan, Yi ; Yang, Hua ; Li, Jingjie ; Feng, Tian ; Ouyang, Yongri ; Jin, Tianbo ; Liu, Ming

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.405-410 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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2
A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population
A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population
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A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

Özcabı, Bahar ; Tahmiscioğlu Bucak, Feride ; Jaferova, Sevinç ; Oruç, Çiğdem ; Adrovic, Amra ; Ceylaner, Serdar ; Ercan, Oya ; Evliyaoğlu, Olcay

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.484-489 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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3
Genetics in Pituitary Short Stature
Genetics in Pituitary Short Stature
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Genetics in Pituitary Short Stature

Uyguner, Z Oya

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2) [Periódico revisado por pares]

Istanbul: Galenos Publishing House

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4
Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia
Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia
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Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia

Papadopoulou, Anna ; Gole, Evangelia ; Melachroinou, Katerina ; Meristoudis, Christos ; Siahanidou, Tania ; Papadimitriou, Anastasios

Journal of clinical research in pediatric endocrinology, 2016-09, Vol.8 (3), p.341-346 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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5
Genetic Approach to Osteoporosis
Genetic Approach to Osteoporosis
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Genetic Approach to Osteoporosis

Alanay, Yasemin

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2) [Periódico revisado por pares]

Istanbul: Galenos Publishing House

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6
Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis
Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis
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Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis

Liu, Shiguo ; Chai, Jian ; Zheng, Guohua ; Li, Huichao ; Lu, Deguo ; Ge, Yinlin

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.21-25 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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7
A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient
A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient
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A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient

Sriphrapradang, Chutintorn ; Thewjitcharoen, Yotsapon ; Chanprasertyothin, Suwannee ; Nakasatien, Soontaree ; Himathongkam, Thep ; Trachoo, Objoon

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.241-245 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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8
The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome
The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome
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The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome

Döneray, Hakan ; Usui, Takeshi ; Kaya, Avni ; Dönmez, Ayşe Sena

Journal of clinical research in pediatric endocrinology, 2015-06, Vol.7 (2), p.140-143 [Periódico revisado por pares]

Turkey: Galenos Publishing House

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9
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

Dursun, Fatma ; Mohamoud, Hussein Sheikh Ali ; Karim, Noreen ; Naeem, Muhammad ; Jelani, Musharraf ; Kırmızıbekmez, Heves

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.472-477 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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10
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy
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Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy

Su, Xueying ; Lin, Ruizhu ; Huang, Yonglan ; Sheng, Huiying ; Li, Xiaofei ; Ting, Tzer Hwu ; Liu, Li ; Li, Xiuzhen Darendeliler,Fatma Feyza

Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.52-57 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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