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Last Updated : 06/20/2022

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Found 7 publications

Pfeiffer syndrome type 3 with FGR2 c.1052C>G (p.Ser351Cys) variant in West Africa: a case report.

Case Report: Anisometropic Astigmatism Secondary to Unilateral Coronal Synostosis.

Facial Dysmorphology in Saethre-Chotzen Syndrome.

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.

Prevalence of cleft lip and palate and associated factors in Brazil's Midwest: a single-center study.

Tracheal cartilaginous sleeve in Pfeiffer syndrome: lesson learnt from its rarity.

Surgical Management of Complex Syndromic Craniosynostosis: Experience With a Rare Genetic Variant.

Showing 1-7 of 7

Last Updated : 06/20/2022