Dalprà L - Search Results

1

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

2

Molecular characterization of FRAXE-positive subjects with mental impairement in two unrelated Italian families.

Russo S, Selicorni A, Bedeschi MF, Natacci F, Viziello P, Fortuna R, Pagani G, Dalprà L, Larizza L. Russo S, et al. Among authors: dalpra l. Am J Med Genet. 1998 Jan 23;75(3):304-8. Am J Med Genet. 1998. PMID: 9475603

3

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

4

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

5

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

6

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. Genet Med. 2005 Nov-Dec;7(9):620-5. doi: 10.1097/01.gim.0000182876.57766.2d. Genet Med. 2005. PMID: 16301863 Free article.

7

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

8

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

9

Different phenotypes in two cases of an apparently identical familial (Yq;13p) translocation.

Doneda L, Magnani I, Tibiletti MG, Dalprà L, Larizza L. Doneda L, et al. Among authors: dalpra l. Hum Reprod. 1992 Apr;7(4):495-9. doi: 10.1093/oxfordjournals.humrep.a137678. Hum Reprod. 1992. PMID: 1522192

10

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

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