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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Clin Res Pediatr Endocrinol
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Galenos Publishing 2015
Gaiak:
Original Article
Sarrera elektronikoa: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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