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99 results
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Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome.
Michelucci A, Ghirri P, Iacopetti P, Conidi ME, Fogli A, Baldinotti F, Lunardi S, Forli F, Moscuzza F, Berrettini S, Boldrini A, Simi P, Pellegrini S. Michelucci A, et al. Among authors: simi p. Int J Pediatr Otorhinolaryngol. 2010 Dec;74(12):1441-4. doi: 10.1016/j.ijporl.2010.09.006. Epub 2010 Oct 12. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20943277
Growth and puberty in Turner's syndrome.
Bertelloni S, Baroncelli GI, Fruzzetti F, Spinelli C, Simi P, Saggese G. Bertelloni S, et al. Among authors: simi p. J Pediatr Endocrinol Metab. 2003 Mar;16 Suppl 2:307-15. J Pediatr Endocrinol Metab. 2003. PMID: 12729409 Review.
Homeobox HOXA10 gene analysis in cryptorchidism.
Bertini V, Bertelloni S, Valetto A, Lala R, Foresta C, Simi P. Bertini V, et al. Among authors: simi p. J Pediatr Endocrinol Metab. 2004 Jan;17(1):41-5. doi: 10.1515/jpem.2004.17.1.41. J Pediatr Endocrinol Metab. 2004. PMID: 14960020
Cx26 gene mutations in idiopathic progressive hearing loss.
Ravecca F, Berrettini S, Forli F, Marcaccini M, Casani A, Baldinotti F, Fogli A, Siciliano G, Simi P. Ravecca F, et al. Among authors: simi p. J Otolaryngol. 2005 Apr;34(2):126-34. doi: 10.2310/7070.2005.04017. J Otolaryngol. 2005. PMID: 16076412
99 results