skip to main content
Refinado por: idioma: Japonês remover idioma: Turco remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia
Material Type:
Artigo
Adicionar ao Meu Espaço

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia

Panzer, Karin ; Ekhaguere, Osayame A ; Darbro, Benjamin ; Cook, Jennifer ; Shchelochkov, Oleg A Darendeliler,Fatma Feyza

Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.70-73 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

Texto completo disponível

2
Turner syndrome and associated problems in Turkish children: a multicenter study
Material Type:
Artigo
Adicionar ao Meu Espaço

Turner syndrome and associated problems in Turkish children: a multicenter study

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 ; Deniz Çakır, Esra ; 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

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1), p.27-36 [Periódico revisado por pares]

Turkey: Galenos Publishing House

Texto completo disponível

3
A case of campomelic dysplasia in whom a new mutation was found in the SOX9 gene
Material Type:
Artigo
Adicionar ao Meu Espaço

A case of campomelic dysplasia in whom a new mutation was found in the SOX9 gene

Karaer, Kadri ; Yüksel, Zafer ; Yalınbaş, Esin ; Scherer, Gerd

Turk Pediatri Arsivi, 2014-06, Vol.49 (2), p.154-156 [Periódico revisado por pares]

Turkey: AVES

Texto completo disponível

Buscando em bases de dados remotas. Favor aguardar.