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Page 1
Temporal bone imaging in GJB2 deafness.
Propst EJ, Blaser S, Stockley TL, Harrison RV, Gordon KA, Papsin BC. Propst EJ, et al. Laryngoscope. 2006 Dec;116(12):2178-86. doi: 10.1097/01.mlg.0000244389.68568.a7. Laryngoscope. 2006. PMID: 17146393 Clinical Trial.
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance.
Chitayat D, Sroka H, Keating S, Colby RS, Ryan G, Toi A, Blaser S, Viero S, Devisme L, Boute-Bénéjean O, Manouvrier-Hanu S, Mortier G, Loeys B, Rauch A, Bitoun P. Chitayat D, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1268-81. doi: 10.1002/ajmg.a.31788. Am J Med Genet A. 2007. PMID: 17506106
Cochleovestibular anomalies in children with cholesteatoma.
Propst EJ, Blaser S, Trimble K, James A, Friedberg J, Papsin BC. Propst EJ, et al. Laryngoscope. 2008 Mar;118(3):517-21. doi: 10.1097/MLG.0b013e31815d8e55. Laryngoscope. 2008. PMID: 18091330 Clinical Trial.
159 results