Dalprà L - Search Results

1

Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis.

Riva P, Crosti F, Orzan F, Dalprà L, Mortini P, Parafioriti A, Pollo B, Fuhrman Conti AM, Miozzo M, Larizza L. Riva P, et al. Among authors: dalpra l. Int J Cancer. 2003 Nov 10;107(3):493-7. doi: 10.1002/ijc.11421. Int J Cancer. 2003. PMID: 14506752 Free article.

2

Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome.

Miozzo M, Castorina P, Riva P, Dalprà L, Fuhrman Conti AM, Volpi L, Hoe TS, Khoo A, Wiegant J, Rosenberg C, Larizza L. Miozzo M, et al. Among authors: dalpra l. Int J Cancer. 1998 Aug 12;77(4):504-10. doi: 10.1002/(sici)1097-0215(19980812)77:4<504::aid-ijc5>3.0.co;2-y. Int J Cancer. 1998. PMID: 9679749 Free article.

3

First cytogenetic study of a recurrent familial chordoma of the clivus.

Dalprà L, Malgara R, Miozzo M, Riva P, Volonte M, Larizza L, Fuhrman Conti AM. Dalprà L, et al. Int J Cancer. 1999 Mar 31;81(1):24-30. doi: 10.1002/(sici)1097-0215(19990331)81:1<24::aid-ijc5>3.0.co;2-o. Int J Cancer. 1999. PMID: 10077147 Free article.

4

A tumor suppressor locus in familial and sporadic chordoma maps to 1p36.

Miozzo M, Dalprà L, Riva P, Volontà M, Macciardi F, Pericotti S, Tibiletti MG, Cerati M, Rohde K, Larizza L, Fuhrman Conti AM. Miozzo M, et al. Among authors: dalpra l. Int J Cancer. 2000 Jul 1;87(1):68-72. Int J Cancer. 2000. PMID: 10861454 Free article.

5

Endometrioid-like yolk sac and Sertoli-Leydig cell tumors in a carrier of a Y heterochromatin insertion into 1qh region: a causal association?

Sala E, Villa N, Crosti F, Miozzo M, Perego P, Cappellini A, Bonazzi C, Barisani D, Dalprà L. Sala E, et al. Among authors: dalpra l. Cancer Genet Cytogenet. 2007 Mar;173(2):164-9. doi: 10.1016/j.cancergencyto.2006.10.014. Cancer Genet Cytogenet. 2007. PMID: 17321334

6

19p deletion in recurring leiomyosarcoma lesions from the same patient.

Riva P, Dalprá L, Gualandri V, Volontè M, Miozzo M, Malgara R, Conti AF, Larizza L. Riva P, et al. Among authors: dalpra l. Cancer Genet Cytogenet. 2000 Jun;119(2):102-8. doi: 10.1016/s0165-4608(99)00222-8. Cancer Genet Cytogenet. 2000. PMID: 10867143

7

Lymph node hyperplasia: clonal chromosomal and genomic rearrangements. Report of two new cases and literature review.

Villa N, Redaelli S, Lissoni S, Saccheri F, Sala E, Crosti F, Dalprà L, Carrino V, Pioltelli P, Isimbaldi G. Villa N, et al. Among authors: dalpra l. Cancer Genet. 2014 Jan-Feb;207(1-2):12-8. doi: 10.1016/j.cancergen.2014.01.003. Epub 2014 Jan 16. Cancer Genet. 2014. PMID: 24636528 Review.

8

Human Chromosome 18 and Acrocentrics: A Dangerous Liaison.

Villa N, Redaelli S, Sala E, Conconi D, Romitti L, Manfredini E, Crosti F, Roversi G, Lavitrano M, Rodeschini O, Recalcati MP, Piazza R, Dalprà L, Riva P, Bentivegna A. Villa N, et al. Among authors: dalpra l. Int J Mol Sci. 2021 May 26;22(11):5637. doi: 10.3390/ijms22115637. Int J Mol Sci. 2021. PMID: 34073228 Free PMC article.

9

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: dalpra l. 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

10

Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome.

Riva P, Castorina P, Manoukian S, Dalprà L, Doneda L, Marini G, den Dunnen J, Larizza L. Riva P, et al. Among authors: dalpra l. Hum Genet. 1996 Dec;98(6):646-50. doi: 10.1007/s004390050277. Hum Genet. 1996. PMID: 8931693

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