Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

OBJECTIVE: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected girls. This study aimed to systematically investigate the key clinical features...

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Dades bibliogràfiques
Publicat a:J Clin Res Pediatr Endocrinol
Autors principals: Yeşilkaya, Ediz, Bereket, Abdullah, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Küçükemre Aydın, Banu, Darcan, Şükran, Dündar, Bumin, Büyükinan, Muammer, Kara, Cengiz, Sarı, Erkan, Adal, Erdal, Akıncı, Ayşehan, Atabek, Mehmet Emre, Demirel, Fatma, Çelik, Nurullah, Özkan, Behzat, Özhan, Bayram, Orbak, Zerrin, Ersoy, Betül, Doğan, Murat, Ataş, Ali, Turan, Serap, Gökşen, Damla, Tarım, Ömer, Yüksel, Bilgin, Ercan, Oya, Hatun, Şükrü, Şimşek, Enver, Ökten, Ayşenur, Abacı, Ayhan, Döneray, Hakan, Özbek, Mehmet Nuri, Keskin, Mehmet, Önal, Hasan, Akyürek, Nesibe, Bulan, Kezban, Tepe, Derya, Emeksiz, Hamdi Cihan, Demir, Korcan, Kızılay, Deniz, Topaloğlu, Ali Kemal, Eren, Erdal, Özen, Samim, Abalı, Saygın, Akın, Leyla, Selver Eklioğlu, Beray, Kaba, Sultan, Anık, Ahmet, Baş, Serpil, Ünüvar, Tolga, Sağlam, Halil, Bolu, Semih, Özgen, Tolga, Doğan, Durmuş, Çakır, Esra Deniz, Şen, Yaşar, Andıran, Nesibe, Çizmecioğlu, Filiz, Evliyaoğlu, Olcay, Karagüzel, Gülay, Pirgon, Özgür, Çatlı, Gönül, Can, Hatice Dilek, Gürbüz, Fatih, Binay, Çiğdem, Baş, Veysel Nijat, Fidancı, Kürşat, Polat, Adem, Gül, Davut, Açıkel, Cengizhan, Demirbilek, Hüseyin, Cinaz, Peyami, Bondy, Carolyn
Format: Artigo
Idioma:Inglês
Publicat: Galenos Publishing 2015
Matèries:
Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4439889/
https://ncbi.nlm.nih.gov/pubmed/25800473
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.1771
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