Università degli studi di Pavia
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Messa publications
Belligni EF, Biamino E, Molinatto C, Messa J, Pierluigi M, Faravelli F, Zuffardi O, Ferrero GB, Silengo MC. Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability.
Ital J Pediatr. 2009 Apr 27;35(1):9.PMID: 19490664
Vetro A, Iasci A, Dal Bello B, Rossi E, Messa J, Montanari L, Cesari S, Zuffardi O. A prenatal case of duplication with terminal deletion of 5p not identified by conventional cytogenetics.
Prenat Diagn. 2008 Dec;28(12):1171-3.
Rossi E, Messa J, Zuffardi O. Ring syndrome: still true?
J Med Genet. 2008 Nov;45(11):766-8. No abstract available. Erratum in: J Med Genet. 2009 Jan;46(1):72.
Rossi E, Riegel M, Messa J, Gimelli S, Maraschio P, Ciccone R, Stroppi M, Riva P, Perrotta CS, Mattina T, Memo L, Baumer A, Kucinskas V, Castellan C, Schinzel A, Zuffardi O. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
J Med Genet. 2008 Mar;45(3):147-54. Epub 2007 Nov 15.
De Gregori M, Ciccone R, Magini P, Pramparo T, Gimelli S, Messa J, Novara F, Vetro A, Rossi E, Maraschio P, Bonaglia MC, Anichini C, Ferrero GB, Silengo M, Fazzi E, Zatterale A, Fischetto R, Previderé C, Belli S, Turci A, Calabrese G, Bernardi F, Meneghelli E, Riegel M, Rocchi M, Guerneri S, Lalatta F, Zelante L, Romano C, Fichera M, Mattina T, Arrigo G, Zollino M, Giglio S, Lonardo F, Bonfante A, Ferlini A, Cifuentes F, Van Esch H, Backx L, Schinzel A, Vermeesch JR, Zuffardi O. Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
J Med Genet. 2007 Dec;44(12):750-62. Epub 2007 Aug 31.
De Gregori M, Pramparo T, Memo L, Gimelli G, Messa J, Rocchi M, Patricelli MG, Ciccone R, Giorda R, Zuffardi O. Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?
Hum Genet. 2005 Nov;118(2):207-13. Epub 2005 Nov 15.
Pramparo T, Grosso S, Messa J, Zatterale A, Bonaglia MC, Chessa L, Balestri P, Rocchi M, Zuffardi O, Giorda R. Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy.
Hum Genet. 2005 Oct;118(1):76-81. Epub 2005 Oct 28
Ital J Pediatr. 2009 Apr 27;35(1):9.PMID: 19490664
Vetro A, Iasci A, Dal Bello B, Rossi E, Messa J, Montanari L, Cesari S, Zuffardi O. A prenatal case of duplication with terminal deletion of 5p not identified by conventional cytogenetics.
Prenat Diagn. 2008 Dec;28(12):1171-3.
Rossi E, Messa J, Zuffardi O. Ring syndrome: still true?
J Med Genet. 2008 Nov;45(11):766-8. No abstract available. Erratum in: J Med Genet. 2009 Jan;46(1):72.
Rossi E, Riegel M, Messa J, Gimelli S, Maraschio P, Ciccone R, Stroppi M, Riva P, Perrotta CS, Mattina T, Memo L, Baumer A, Kucinskas V, Castellan C, Schinzel A, Zuffardi O. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
J Med Genet. 2008 Mar;45(3):147-54. Epub 2007 Nov 15.
De Gregori M, Ciccone R, Magini P, Pramparo T, Gimelli S, Messa J, Novara F, Vetro A, Rossi E, Maraschio P, Bonaglia MC, Anichini C, Ferrero GB, Silengo M, Fazzi E, Zatterale A, Fischetto R, Previderé C, Belli S, Turci A, Calabrese G, Bernardi F, Meneghelli E, Riegel M, Rocchi M, Guerneri S, Lalatta F, Zelante L, Romano C, Fichera M, Mattina T, Arrigo G, Zollino M, Giglio S, Lonardo F, Bonfante A, Ferlini A, Cifuentes F, Van Esch H, Backx L, Schinzel A, Vermeesch JR, Zuffardi O. Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
J Med Genet. 2007 Dec;44(12):750-62. Epub 2007 Aug 31.
De Gregori M, Pramparo T, Memo L, Gimelli G, Messa J, Rocchi M, Patricelli MG, Ciccone R, Giorda R, Zuffardi O. Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?
Hum Genet. 2005 Nov;118(2):207-13. Epub 2005 Nov 15.
Pramparo T, Grosso S, Messa J, Zatterale A, Bonaglia MC, Chessa L, Balestri P, Rocchi M, Zuffardi O, Giorda R. Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy.
Hum Genet. 2005 Oct;118(1):76-81. Epub 2005 Oct 28
