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Inheritance of Niikawa-Kuroki (Kabuki makeup) syndrome.
Silengo M, Lerone M, Seri M, Romeo G. Silengo M, et al. Am J Med Genet. 1996 Dec 18;66(3):368. doi: 10.1002/(SICI)1096-8628(19961218)66:3<368::AID-AJMG28>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8985504 No abstract available.
Ectodermal abnormalities in Kabuki syndrome.
Lerone M, Priolo M, Naselli A, Vignolo M, Romeo G, Silengo MC. Lerone M, et al. Among authors: silengo mc. Am J Med Genet. 1997 Dec 19;73(3):263-6. doi: 10.1002/(sici)1096-8628(19971219)73:3<263::aid-ajmg6>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9415681 Review.
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.
Seri M, Cusano R, Forabosco P, Cinti R, Caroli F, Picco P, Bini R, Morra VB, De Michele G, Lerone M, Silengo M, Pela I, Borrone C, Romeo G, Devoto M. Seri M, et al. Among authors: silengo m. Am J Hum Genet. 1999 Feb;64(2):586-93. doi: 10.1086/302241. Am J Hum Genet. 1999. PMID: 9973297 Free PMC article.
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?
Bohring A, Silengo M, Lerone M, Superneau DW, Spaich C, Braddock SR, Poss A, Opitz JM. Bohring A, et al. Among authors: silengo m. Am J Med Genet. 1999 Aug 27;85(5):438-46. doi: 10.1002/(sici)1096-8628(19990827)85:5<438::aid-ajmg2>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10405439 Review.
Fontaine-Farriaux craniosynostosis: second report in the literature.
Priolo M, De Toni T, Baffico M, Cama A, Seri M, Cusano R, Costabello L, Fondelli P, Capra V, Silengo M, Ravazzolo R, Lerone M. Priolo M, et al. Among authors: silengo m. Am J Med Genet. 2001 May 1;100(3):214-8. Am J Med Genet. 2001. PMID: 11343306
154 results