Mattina T - Search Results

1

Incorpora G, Cocuzza M, Mattina T. Incorpora G, et al. Among authors: mattina t. Am J Med Genet. 1994 Aug 15;52(2):246-7. doi: 10.1002/ajmg.1320520229. Am J Med Genet. 1994. PMID: 7802023 No abstract available.

2

Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.

Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G. Gangarossa S, et al. Among authors: mattina t. Am J Med Genet. 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8882392

3

Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.

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. Rossi E, et al. Among authors: mattina t. J Med Genet. 2008 Mar;45(3):147-54. doi: 10.1136/jmg.2007.054007. Epub 2007 Nov 15. J Med Genet. 2008. PMID: 18006671 Free article.

4

Small 4p16.3 deletions: Three additional patients and review of the literature.

Bernardini L, Radio FC, Acquaviva F, Gorgone C, Postorivo D, Torres B, Alesi V, Magliozzi M, Lonardo F, Monica MD, Nardone AM, Cesario C, Mattina T, Scarano G, Dallapiccola B, Digilio MC, Novelli A. Bernardini L, et al. Among authors: mattina t. Am J Med Genet A. 2018 Nov;176(11):2501-2508. doi: 10.1002/ajmg.a.40512. Epub 2018 Sep 23. Am J Med Genet A. 2018. PMID: 30244530 Review.

5

RFLP analysis in 5 Sicilian families with the fragile X syndrome.

Romano V, Mascali G, Chiavetta V, Ragusa RM, Barletta C, Romano C, Mollica F, Mattina T, Gross A, Brown WT, et al. Romano V, et al. Among authors: mattina t. Am J Med Genet. 1991 Feb-Mar;38(2-3):347-8. doi: 10.1002/ajmg.1320380236. Am J Med Genet. 1991. PMID: 1673309 No abstract available.

6

The fragile X in Sicily: an epidemiological survey.

Neri G, Sanfilippo S, Pavone L, Mollica F, Barberi I, Giuffrè L, Romano C, Mattina T, Cammarata M, Ragusa MG, et al. Neri G, et al. Among authors: mattina t. Am J Med Genet. 1988 May-Jun;30(1-2):665-72. doi: 10.1002/ajmg.1320300167. Am J Med Genet. 1988. PMID: 3177477

7

Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.

Mattina T, Pierluigi M, Mazzone D, Scardilli S, Perfumo C, Mollica F. Mattina T, et al. J Med Genet. 1997 Nov;34(11):945-8. doi: 10.1136/jmg.34.11.945. J Med Genet. 1997. PMID: 9391894 Free PMC article.

8

The 11q terminal deletion disorder: a prospective study of 110 cases.

Grossfeld PD, Mattina T, Lai Z, Favier R, Jones KL, Cotter F, Jones C. Grossfeld PD, et al. Among authors: mattina t. Am J Med Genet A. 2004 Aug 15;129A(1):51-61. doi: 10.1002/ajmg.a.30090. Am J Med Genet A. 2004. PMID: 15266616

9

Narrowing the deleted region associated with the 15q21 syndrome.

Pramparo T, Mattina T, Gimelli S, Liehr T, Zuffardi O. Pramparo T, et al. Among authors: mattina t. Eur J Med Genet. 2005 Jul-Sep;48(3):346-52. doi: 10.1016/j.ejmg.2005.04.012. Eur J Med Genet. 2005. PMID: 16179230

10

Gene-targeted deletion in mice of the Ets-1 transcription factor, a candidate gene in the Jacobsen syndrome kidney "critical region," causes abnormal kidney development.

Ye M, Xu L, Fu M, Chen D, Mattina T, Zufardi O, Rossi E, Bush KT, Nigam SK, Grossfeld P. Ye M, et al. Among authors: mattina t. Am J Med Genet A. 2019 Jan;179(1):71-77. doi: 10.1002/ajmg.a.40481. Epub 2018 Nov 13. Am J Med Genet A. 2019. PMID: 30422383

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