Rezultati - Halil Sağlam
- Showing 1 - 3 results of 3
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1
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism od Hakan Cangül, Xiao-Hui Liao, Erik Schoenmakers, Jukka Kero, Sharon Barone, Panudda Srichomkwun, Hideyuki Iwayama, Eva Serra, Halil Sağlam, Erdal Eren, Ömer Tarım, Adeline K. Nicholas, Ilona Zvetkova, Carl A. Anderson, Fiona E. Karet, Kristien Boelaert, Marja Ojaniemi, Jarmo Jääskeläinen, Konrad Patyra, Christoffer Löf, E. D. Williams, Manoocher Soleimani, Timothy Barrett, Eamonn R. Maher, Krishna Chatterjee, Samuel Refetoff, Nadia Schoenmakers
Izdano 2018Artigo -
2
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ od Adeline K. Nicholas, Eva Serra, Hakan Cangül, Saif Al-Yaarubi, Irfan Ullah, Erik Schoenmakers, Asma Deeb, Abdelhadi Habeb, Mohammad S. Al-Maghamsi, Catherine Peters, Nisha Nathwani, Zehra Aycan, Halil Sağlam, Ece Böber, Mehul Dattani, Savitha Shenoy, Philip Murray, Amir Babiker, Ruben H. Willemsen, Ajay Thankamony, Greta Lyons, Rachael Irwin, Raja Padidela, Kavitha Tharian, Justin H. Davies, Vijith Puthi, Soo‐Mi Park, Ahmed F. Massoud, John W Gregory, Assunta Albanese, Evelien Pease-Gevers, Howard Martin, Kim Brügger, Eamonn R. Maher, Krishna Chatterjee, Carl A. Anderson, Nadia Schoenmakers
Izdano 2016Artigo -
3
Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study od Ediz Yeşilkaya, Abdullah Bereket, Feyza Darendelıler, Firdevs Baş, Şükran Poyrazoğlu, Banu Küçükemre Aydın, Şükran Darcan, Bumin Nuri Dündar, Muammer Büyükinan, Cengiz Kara, Erkan Sarı, Erdal Adal, Ayşehan Akıncı, Mehmet Emre Atabek, Fatma Demirel, Nurullah Çelik, Behzat Özkan, Bayram Özhan, Zerrin Orbak, Betül Ersoy, Murat Doğan, Ali Ataş, Serap Turan, Damla Gökşen, Ömer Tarım, Bilgin Yüksel, Oya Ercan, Şükrü Hatun, Enver Şimşek, Ayşenur Ökten, Ayhan Abacı, Hakan Döneray, Mehmet Nuri Özbek, Mehmet Keskın, Hasan Önal, Nesibe Akyürek, Kezban Bulan, Derya Tepe, Hamdi Cihan Emeksiz, Korcan Demir, Deniz Özalp Kızılay, A. Kemal Topaloğlu, Erdal Eren, Samim Özen, Saygın Abalı, Leyla Akın, Beray Selver Eklioğlu, Sultan Kaba, Ahmet Anık, Serpil Baş, Tolga Ünüvar, Halil Sağlam, Semih Bolu, İlker Tolga Özgen, Durmuş Doğan, Esra Deniz Papatya Çakır, Yaşar Şen, Nesibe Andıran, Filiz Çizmecioğlu, Olcay Evliyaoğlu, Gülay Karagüzel, Özgür Pirgon, Gönül Çatlı, Hatice Dilek Can, Fatih Gürbüz, Çiğdem Binay, Veysel Nijat Baş, Kürşat Fidancı, Adem Polat, Davut Gül, Cengizhan Açıkel, Hüseyin Demirbilek, Peyamı Cınaz, Carolyn A. Bondy
Izdano 2015Artigo
Iskalna orodja:
Sorodne teme
Biology
Gene
Genetics
Internal medicine
Medicine
Congenital hypothyroidism
Thyroid
Aortic valve
Bicuspid aortic valve
Chemistry
Chromosome
Diiodotyrosine
Endocrinology
Environmental health
Etiology
Gastroenterology
Genetic heterogeneity
Goiter
Gynecology
Hormone
In silico
Iodide
Iodine
Karyotype
Mutation
Organic chemistry
Outpatient clinic
Pediatrics
Pendrin
Phenotype