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Pediatrics International : Official Journal of the Japan Pediatric Society|November 30, 2007
Effect of zinc sulfate on common cold in children: randomized, double blind studyZafer Kurugöl, Nuri Bayram, Tahir AtikTurk Pediatri Arsivi|August 5, 2016
A rare sex chromosome aneuploidy: 48,XXYY syndromeTahir Atik, Özgür Çoğulu, Ferda ÖzkınayTurk Pediatri Arsivi|February 28, 2018
Two patients with Apert syndrome with different mutations: the importance of early diagnosisEsra Işık, Tahir Atik, Hüseyin Onay, et al.International Journal of Pediatric Otorhinolaryngology|January 27, 2016
Mannose binding lectin codon 54 polymorphism and susceptibility to recurrent respiratory tract infections in children: A meta-analysisOzlem Atan, Ahmet Kucukcelebi, Tahir Atik, et al.American Journal of Medical Genetics. Part A|December 10, 2014
A new patient with LACHT syndrome (Mardini-Nyhan association)Tahir Atik, Huseyin Ozan Torun, Ozgur Cogulu, et al.European Journal of Medical Genetics|September 24, 2018
Biallelic TOR1A mutations cause severe arthrogryposis: A case requiring reverse phenotypingEsra Isik, Ayca Aykut, Tahir Atik, et al.Journal of Tropical Pediatrics|January 11, 2014
A new mutation in the TBX5 gene in Holt-Oram syndrome: two cases in the same family and prenatal diagnosisTahir Atik, Huseyin Dervisoglu, Huseyin Onay, et al.Clinical Neurology and Neurosurgery|August 21, 2021
Mutation spectrum of the NF1 gene and genotype-phenotype correlations in Turkish patients: Seventeen novel pathogenic variantsAsli Ece Solmaz, Esra Isik, Tahir Atik, et al.Clinical Neurology and Neurosurgery|July 1, 2018
Clinical and genetic features of L1 syndrome patients: Definition of two novel mutationsEsra Isik, Huseyin Onay, Tahir Atik, et al.Genetics Research|April 1, 2015
Whole-exome sequencing and its impact in hereditary hearing lossTahir Atik, Guney Bademci, Oscar Diaz-Horta, et al.Pageof 10