Dalprá L - Search Results

1

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

2

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

3

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

4

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

5

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

6

Prenatal diagnosis of an extranumerary i(22p) with normal phenotype.

Doneda L, Dalprà L, Tibiletti MG, Larizza L. Doneda L, et al. Among authors: dalpra l. Ann Genet. 1993;36(3):154-8. Ann Genet. 1993. PMID: 8117060

7

Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndrome.

Castorina P, Selicorni A, Bedeschi F, Dalprà L, Larizza L. Castorina P, et al. Among authors: dalpra l. Am J Med Genet. 1997 Mar 3;69(1):107-11. doi: 10.1002/(sici)1096-8628(19970303)69:1<107::aid-ajmg21>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9066894

8

Expression of three rare fragile sites: chromosomal truncation, amplification of distal segment and telomeric renewal.

Villa N, Dalprà L, Larizza L. Villa N, et al. Among authors: dalpra l. Chromosoma. 1997 Nov;106(6):400-4. doi: 10.1007/s004120050261. Chromosoma. 1997. PMID: 9362548

9

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

10

A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency.

Pallotta R, Dalprà L, Miozzo M, Ehresmann T, Fusilli P. Pallotta R, et al. Among authors: dalpra l. Am J Med Genet. 2001 Dec 15;104(4):282-6. doi: 10.1002/ajmg.10068. Am J Med Genet. 2001. PMID: 11754060

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