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Genetic Counseling (Geneva, Switzerland)|February 9, 2016
OROFACIAL FINDINGS AND DENTAL MANAGEMENT OF WILLIAMS SYNDROMED Cogulu, F Hazan, F Cagirir DindarogluBalkan Journal of Medical Genetics : BJMG|October 28, 2016
Sarcolemmal deficiency of sarcoglycan complex in an 18-month-old Turkish boy with a large deletion in the beta sarcoglycan geneG Diniz, H Tekgul, F Hazan, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A cardio-facio-cutaneous syndrome case with tight Achilles tendonsF Hazan, A Aykut, M Hizarcioglu, et al.Journal of Endocrinological Investigation|November 15, 2021
Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7S Acar, S Gürsoy, G Arslan, et al.Acta Endocrinologica (Bucharest, Romania : 2005)|June 1, 2019
SCREENING OF PROP-1, LHX2 AND POU1F1 MUTATIONS IN PATIENTS WITH ECTOPIC POSTERIOR PITUITARY GLANDH A Korkmaz, U Karaarslan, C Eraslan, et al.Pageof 1