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Single median maxillary central incisor syndrome and variant in SMO gene associated with SHH pathway.
Zatoński T, Pazdro-Zastawny K, Morawska-Kochman M, Biela M, Kołtowska A, Rydzanicz M, Rozensztrauch A, Kosińska J, Dorobisz K, Płoski R, Śmigiel R. Zatoński T, et al. Among authors: rozensztrauch a. Int J Pediatr Otorhinolaryngol. 2020 Jul;134:110038. doi: 10.1016/j.ijporl.2020.110038. Epub 2020 Apr 13. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32335464
The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes.
Wolańska E, Pollak A, Rydzanicz M, Pesz K, Kłaniewska M, Rozensztrauch A, Skiba P, Stawiński P, Płoski R, Śmigiel R. Wolańska E, et al. Among authors: rozensztrauch a. Genes (Basel). 2021 Feb 27;12(3):350. doi: 10.3390/genes12030350. Genes (Basel). 2021. PMID: 33673493 Free PMC article.
Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.
Klaniewska M, Toczewski K, Rozensztrauch A, Bloch M, Dzielendziak A, Gasperowicz P, Slezak R, Ploski R, Rydzanicz M, Smigiel R, Patkowski D. Klaniewska M, et al. Among authors: rozensztrauch a. Front Pediatr. 2021 Dec 2;9:783553. doi: 10.3389/fped.2021.783553. eCollection 2021. Front Pediatr. 2021. PMID: 34926353 Free PMC article.
26 results