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5 ensaios clínicos encontrados, 3 ativos.
Prenatal diagnosis of Pfeiffer syndrome type 2 with increased nuchal translucency.
Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages.
Pfeiffer Syndrome type 2; A case report of cranio-orbitofaciostenosis with bilateral choanal atresia at Muhimbili National Hospital, Tanzania.
Pfeiffer type 2 syndrome: review with updates on its genetics and molecular biology.
Pfeiffer type 2 syndrome: review with updates on its genetics and molecular biology.