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2005 | 2 |
2006 | 1 |
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2020 | 1 |
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Page 1
Cytogenetics of premature ovarian failure: an investigation on 269 affected women.
J Biomed Biotechnol. 2011;2011:370195. doi: 10.1155/2011/370195. Epub 2011 Jan 17.
J Biomed Biotechnol. 2011.
PMID: 21318170
Free PMC article.
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
Redaelli S, Grati FR, Tritto V, Giannuzzi G, Recalcati MP, Sala E, Villa N, Crosti F, Roversi G, Malvestiti F, Zanatta V, Repetti E, Rodeschini O, Valtorta C, Catusi I, Romitti L, Martinoli E, Conconi D, Dalprà L, Lavitrano M, Riva P, Bentivegna A.
Redaelli S, et al. Among authors: martinoli e.
HGG Adv. 2024 Apr 11;5(2):100261. doi: 10.1016/j.xhgg.2023.100261. Epub 2023 Dec 30.
HGG Adv. 2024.
PMID: 38160254
Free PMC article.
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Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes. Report of 24 Unrelated Cases.
Redaelli S, Conconi D, Villa N, Sala E, Crosti F, Corti C, Catusi I, Garzo M, Romitti L, Martinoli E, Patrizi A, Malgara R, Recalcati MP, Dalprà L, Lavitrano M, Riva P, Roversi G, Bentivegna A.
Redaelli S, et al. Among authors: martinoli e.
Int J Mol Sci. 2020 May 13;21(10):3431. doi: 10.3390/ijms21103431.
Int J Mol Sci. 2020.
PMID: 32413994
Free PMC article.
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Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories.
Dalprà L, Giardino D, Finelli P, Corti C, Valtorta C, Guerneri S, Ilardi P, Fortuna R, Coviello D, Nocera G, Amico FP, Martinoli E, Sala E, Villa N, Crosti F, Chiodo F, di Cantogno LV, Savin E, Croci G, Franchi F, Venti G, Donti E, Migliori V, Pettinari A, Bonifacio S, Centrone C, Torricelli F, Rossi S, Simi P, Granata P, Casalone R, Lenzini E, Artifoni L, Pecile V, Barlati S, Bellotti D, Caufin D, Police A, Cavani S, Piombo G, Pierluigi M, Larizza L.
Dalprà L, et al. Among authors: martinoli e.
Genet Med. 2005 Nov-Dec;7(9):620-5. doi: 10.1097/01.gim.0000182876.57766.2d.
Genet Med. 2005.
PMID: 16301863
Free article.
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Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements.
Portera G, Venturin M, Patrizi A, Martinoli E, Riva P, Dalprà L.
Portera G, et al. Among authors: martinoli e.
J Hum Genet. 2006;51(1):68-75. doi: 10.1007/s10038-005-0326-9. Epub 2005 Dec 3.
J Hum Genet. 2006.
PMID: 16328081
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A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome.
Martinoli E, Zuccotti GV, Pogliani L, Volontè M, Venturin M, Fortina P, Ertel A, Redaelli S, Riva P, Dalprà L.
Martinoli E, et al.
Am J Med Genet A. 2010 Apr;152A(4):1043-5. doi: 10.1002/ajmg.a.33335.
Am J Med Genet A. 2010.
PMID: 20358625
No abstract available.
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De novo balanced chromosome rearrangements in prenatal diagnosis.
Giardino D, Corti C, Ballarati L, Colombo D, Sala E, Villa N, Piombo G, Pierluigi M, Faravelli F, Guerneri S, Coviello D, Lalatta F, Cavallari U, Bellotti D, Barlati S, Croci G, Franchi F, Savin E, Nocera G, Amico FP, Granata P, Casalone R, Nutini L, Lisi E, Torricelli F, Giussani U, Facchinetti B, Guanti G, Di Giacomo M, Susca FP, Pecile V, Romitti L, Cardarelli L, Racalbuto E, Police MA, Chiodo F, Rodeschini O, Falcone P, Donti E, Grimoldi MG, Martinoli E, Stioui S, Caufin D, Lauricella SA, Tanzariello SA, Voglino G, Lenzini E, Besozzi M, Larizza L, Dalprà L.
Giardino D, et al. Among authors: martinoli e.
Prenat Diagn. 2009 Mar;29(3):257-65. doi: 10.1002/pd.2215.
Prenat Diagn. 2009.
PMID: 19248039
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