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Autor:
Kılavuz S; Division of Pediatric Metabolism and Nutrition, Department of Pediatrics, Faculty of Medicine, Çukurova University,, Adana, Turkey., Basaran S; Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Çukurova University, Adana, Turkey., Kor D; Division of Pediatric Metabolism and Nutrition, Department of Pediatrics, Faculty of Medicine, Çukurova University,, Adana, Turkey., Bulut FD; Division of Pediatric Metabolism and Nutrition, Department of Pediatrics, Faculty of Medicine, Çukurova University,, Adana, Turkey., Erdem S; Division of Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine, Çukurova University, Adana, Turkey., Ballı HT; Department of Radiology, Faculty of Medicine, Çukurova University, Adana, Turkey., Dağkıran M; Department of Ear, Nose and Throat Diseases, Faculty of Medicine, Çukurova University, Adana, Turkey., Bisgin A; Medical Genetics Department of Medical Faculty, Cukurova University AGENTEM (Adana Genetic Diseases Diagnosis and Treatment Center), Adana, Turkey., Mungan HNÖ; Division of Pediatric Metabolism and Nutrition, Department of Pediatrics, Faculty of Medicine, Çukurova University, 01130, Sarıçam, Adana, Turkey. munganhno@gmail.com.
Publikováno v:
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2021 Mar 22; Vol. 16 (1), pp. 144. Date of Electronic Publication: 2021 Mar 22.