Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism
Kotan, Leman Damla, Ternier, Gaetan, Cakir, Aydilek Dagdeviren, Emeksiz, Hamdi Cihan, Turan, Ihsan, Delpouve, Gaspard, De Kardelen, Asli rya, Ozcabi, Bahar, Isik, Emregul, Mengen, Eda, De Cakir, Esra niz P., Yuksel, Aysegul, Agladioglu, Sebahat Yilmaz, Dilek, Semine Ozdemir, Evliyaoglu, Olcay, Darendeliler, Feyza, Gurbuz, Fatih, Akkus, Gamze, Yuksel, Bilgin, Giacobini, Paolo, Topaloglu, A. Kemal
Published in Genetics in medicine (01.06.2021)
Published in Genetics in medicine (01.06.2021)
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Journal Article
Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism
Kotan, Leman Damla, Ternier, Gaetan, Cakir, Aydilek Dagdeviren, Emeksiz, Hamdi Cihan, Turan, ihsan, Delpouve, Gaspard, Kardelen, Asli Derya, Ozcabi, Bahar, Isik, Emregul, Mengen, Eda, Cakir, Esra Deniz P., Yuksel, Aysegul, Agladioglu, Sabahat Yilmaz, Dilek, Semine Ozdemir, Evliyaoglu, Olcay, Darendeliler, Feyza, Gurbuz, Fatih, Akkus, Gamze, Yuksel, Bilgin, Giacobini, Paolo, Kemal Topaloglu, A.
Published in Genetics in medicine (25.01.2021)
Published in Genetics in medicine (25.01.2021)
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Evaluation of the patients with congenital hypothyroidism: effect of the national screening program/Konjenital hipotiroidili olgularin degerlendirilmesi: ulusal tarama programinin etkisi
Eren, Erdal, Saglam, Halil, Zengin, Aysel, Gul, Yahya, Cakir, Esra Deniz P, Ozgur, Taner, Tarim, Omer
Published in Güncel pediatri (01.04.2011)
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Published in Güncel pediatri (01.04.2011)
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