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Radiographic findings in Wiedemann-Rautenstrauch syndrome.
Obregon MG, Bergami GL, Giannotti A, Digilio MC, Virgili Q, Guadagni AM, Pompei E, Dallapiccola B. Obregon MG, et al. Pediatr Radiol. 1992;22(6):474-5. doi: 10.1007/BF02013521. Pediatr Radiol. 1992. PMID: 1437383
Familial postaxial acrofacial dysostosis syndrome.
Giannotti A, Digilio MC, Virgili Q, Obregon MG, Guadagni AM, Ventura T, Dallapiccola B. Giannotti A, et al. Among authors: obregon mg. J Med Genet. 1992 Oct;29(10):752. doi: 10.1136/jmg.29.10.752. J Med Genet. 1992. PMID: 1433242 Free PMC article. No abstract available.
Discrete membranous subaortic stenosis in siblings.
Digilio MC, Giannotti A, Marino B, Obregon MG, Dallapiccola B. Digilio MC, et al. Among authors: obregon mg. Eur J Pediatr. 1993 Jul;152(7):622. doi: 10.1007/BF01954097. Eur J Pediatr. 1993. PMID: 8354327 No abstract available.
Interstitial deletion del(17) (q21.3q23 or 24.2) syndrome.
Dallapiccola B, Mingarelli R, Digilio C, Obregon MG, Giannotti A. Dallapiccola B, et al. Among authors: obregon mg. Clin Genet. 1993 Jan;43(1):54-5. doi: 10.1111/j.1399-0004.1993.tb04452.x. Clin Genet. 1993. PMID: 8462199 No abstract available.
Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants.
Kortüm F, Niceta M, Magliozzi M, Dumic Kubat K, Robertson SP, Moresco A, Dentici ML, Baban A, Leoni C, Onesimo R, Obregon MG, Digilio MC, Zampino G, Novelli A, Tartaglia M, Kutsche K. Kortüm F, et al. Among authors: obregon mg. Eur J Med Genet. 2020 Sep;63(9):103996. doi: 10.1016/j.ejmg.2020.103996. Epub 2020 Jul 2. Eur J Med Genet. 2020. PMID: 32622958
46 results