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Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.
Garavelli L, Donadio A, Zanacca C, Banchini G, Della Giustina E, Bertani G, Albertini G, Del Rossi C, Zweier C, Rauch A, Zollino M, Neri G. Garavelli L, et al. Among authors: albertini g. Am J Med Genet A. 2003 Feb 1;116A(4):385-8. doi: 10.1002/ajmg.a.10855. Am J Med Genet A. 2003. PMID: 12522797 No abstract available.
Holt-Oram syndrome associated with anomalies of the feet.
Garavelli L, De Brasi D, Verri R, Guareschi E, Cariola F, Melis D, Calcagno G, Salvatore F, Unger S, Sebastio G, Albertini G, Rivieri F, Soli F, Superti-Furga A, Gentile M. Garavelli L, et al. Among authors: albertini g. Am J Med Genet A. 2008 May 1;146A(9):1185-9. doi: 10.1002/ajmg.a.32170. Am J Med Genet A. 2008. PMID: 18351627
Oral dyskinesia induced by fluoxetine therapy for infantile autism.
Albertini G, Majolini L, Di Gennaro G, Quarato P, Scoppetta C, Onorati P, Albertini G, Majolini L, Di Gennaro G, Quarato P, Scoppetta C, Onorati P, Albertini G, Majolini L, Di Gennaro G, Quarato P, Scoppetta C, Onorati P. Albertini G, et al. Pediatr Neurol. 2004 Jul;31(1):76. doi: 10.1016/j.pediatrneurol.2004.02.002. Pediatr Neurol. 2004. PMID: 15246500 No abstract available.
Ultrasonographic characterization of parametrial endometriosis: a prospective study.
Barra F, Zorzi C, Albanese M, De Mitri P, Stepniewska A, Roviglione G, Giani M, Albertini G, Ferrero S, Ceccaroni M. Barra F, et al. Among authors: albertini g. Fertil Steril. 2024 Jul;122(1):150-161. doi: 10.1016/j.fertnstert.2024.02.031. Epub 2024 Feb 19. Fertil Steril. 2024. PMID: 38382700 Free article.
240 results