ISSN:1308-5727 E-ISSN:1308-5735

Original Article

Identification of Novel ROR2 Gene Mutations in Indian Children with Robinow Syndrome
  • Parag M Tamhankar
  • Lakshmi Vasudevan
  • Shweta Kondurkar
  • Yashaswini K
  • Sunil Kumar Agarwalla
  • Mohandas Nair
  • Ramkumar TV
  • Nitin Chaubal
  • Vasundhara Sridhar Chennuri
J Clin Res Pediatr Endocrinol 2014; 6: 79-83 DOI: 10.4274/jcrpe.1233 PMID:24932600
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Parental Perception of Terminology of Disorders of Sex Development in Western Turkey
  • Sibel Tiryaki
  • Ali Tekin
  • İsmail Yağmur
  • Samim Özen
  • Burcu Özbaran
  • Damla Gökşen
  • Şükran Darcan
  • İbrahim Ulman
  • Ali Avanoğlu
J Clin Res Pediatr Endocrinol 2018; 10: 216-222 DOI: 10.4274/jcrpe.0007 PMID:29595517
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Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges
  • Fatih Gürbüz
  • Murat Alkan
  • Gonca Çelik
  • Atıl Bişgin
  • Necmi Çekin
  • İlker Ünal
  • Ali Kemal Topaloğlu
  • Ünal Zorludemir
  • Ayşe Avcı
  • Bilgin Yüksel
J Clin Res Pediatr Endocrinol 2020; 12: 347-357 DOI: 10.4274/jcrpe.galenos.2020.2020.0009 PMID:32212580
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Case Report

Ring Chromosome 13 and Ambiguous Genitalia
  • Elif Özsu
  • Gül Yeşiltepe Mutlu
  • Belkıs İpekçi
J Clin Res Pediatr Endocrinol 2014; 6: 122-124 DOI: 10.4274/jcrpe.1194 PMID:24932608
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A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect
  • Tülay Güran
  • Gözde Yeşil
  • Ömer Güran
  • Suna Cesur
  • Oktav Bosnalı
  • Ayşenur Celayir
  • Sevilay Topçuoğlu
  • Abdullah Bereket
J Clin Res Pediatr Endocrinol 2012; 4: 151-153 DOI: 10.4274/Jcrpe.685 PMID:22664361
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Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene
  • Asma Deeb
  • Hana Al Suwaidi
  • Fakunle Ibukunoluwa
  • Salima Attia
J Clin Res Pediatr Endocrinol 2016; 8: 236-240 DOI: 10.4274/jcrpe.2782 PMID:27086719
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Case Report

Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene
  • Edip Unal
  • Ruken Yıldırım
  • Funda Feryal Taş
  • Vasfiye Demir
  • Hüseyin Onay
  • Yusuf Kenan Haspolat
J Clin Res Pediatr Endocrinol 2018; 10: 377-381 DOI: 10.4274/jcrpe.0011 PMID:29553041
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Latest Update: 15.01.2021
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