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Author/Creator Gurbuz, Fatih

1. An emerging, recognizable facial phenotype in association with mutations in GLI‐similar 3 (GLIS3). Issue 7 (5th May 2016)

Authors:
Dimitri, Paul; De Franco, Elisa; Habeb, Abdelhadi M.; Gurbuz, Fatih; Moussa, Khairya; Taha, Doris; Wales, Jerry K. H.; Hogue, Jacob; Slavotinek, Anne; Shetty, Ambika; Balasubramanian, Meena
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 7(2016)
Page Start:
1918
Record Type:
Journal Article
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4. Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families. (7th November 2014)

Authors:
Demirbilek, Huseyin; Ozbek, M. Nuri; Demir, Korcan; Kotan, L. Damla; Cesur, Yasar; Dogan, Murat; Temiz, Fatih; Mengen, Eda; Gurbuz, Fatih; Yuksel, Bilgin; Topaloglu, A. Kemal
Journal:
Clinical endocrinology
Issue:
Volume 82:Number 3(2015:Mar.)
Page Start:
429
Record Type:
Journal Article
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5. PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism. (16th February 2022)

Authors:
Welch, Bradley A.; Cho, Hyun‐ju; Ucakturk, Seyit Ahmet; Farmer, Stephen Matthew; Cetinkaya, Semra; Abaci, Ayhan; Akkus, Gamze; Simsek, Enver; Kotan, Leman Damla; Turan, Ihsan; Gurbuz, Fatih; Yuksel, Bilgin; Wray, Susan; Topaloglu, A. Kemal
Journal:
Journal of neuroendocrinology
Issue:
Volume 34:Number 4(2022)
Page Start:
n/a
Record Type:
Journal Article
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