Dellavecchia C - Search Results

1

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

Floridia G, Piantanida M, Minelli A, Dellavecchia C, Bonaglia C, Rossi E, Gimelli G, Croci G, Franchi F, Gilgenkrantz S, Grammatico P, Dalprá L, Wood S, Danesino C, Zuffardi O. Floridia G, et al. Among authors: dellavecchia c. Am J Hum Genet. 1996 Apr;58(4):785-96. Am J Hum Genet. 1996. PMID: 8644743 Free PMC article.

2

Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?

Piantanida M, Dellavecchia C, Floridia G, Giglio S, Hoeller H, Dordi B, Danesino C, Schinzel A, Zuffardi O. Piantanida M, et al. Among authors: dellavecchia c. Hum Genet. 1997 Jun;99(6):766-71. doi: 10.1007/s004390050445. Hum Genet. 1997. PMID: 9187670

3

Ring chromosome 13 with loss of the region D13S317-D13S285: phenotypic overlap with XK syndrome.

Guala A, Dellavecchia C, Mannarino S, Rognone F, Giglio S, Minelli A, Danesino C. Guala A, et al. Among authors: dellavecchia c. Am J Med Genet. 1997 Oct 31;72(3):319-23. Am J Med Genet. 1997. PMID: 9332662 Review.

4

Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.

Piantanida M, Buscarini E, Dellavecchia C, Minelli A, Rossi A, Buscarini L, Danesino C. Piantanida M, et al. Among authors: dellavecchia c. J Med Genet. 1996 Jun;33(6):441-3. doi: 10.1136/jmg.33.6.441. J Med Genet. 1996. PMID: 8782041 Free PMC article.

5

Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss.

Seghezzi L, Dellavecchia C, Maserati E, Minelli A, Carrà A, Locatelli F, Argusti A, Lo Curto F, Danesino C, Pasquali F. Seghezzi L, et al. Among authors: dellavecchia c. Cancer Genet Cytogenet. 1997 Nov;99(1):77-80. doi: 10.1016/s0165-4608(96)00431-1. Cancer Genet Cytogenet. 1997. PMID: 9352800

6

Early onset of gastric carcinoma and constitutional deletion of 18p.

Dellavecchia C, Guala A, Olivieri C, Haintink O, Cadario F, Luinetti O, Fiocca R, Minelli A, Danesino C, Bona G. Dellavecchia C, et al. Cancer Genet Cytogenet. 1999 Aug;113(1):96-9. doi: 10.1016/s0165-4608(99)00003-5. Cancer Genet Cytogenet. 1999. PMID: 10459356

7

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C, Sujansky E, Dallapiccola B, Zuffardi O. Giglio S, et al. Among authors: dellavecchia c. Circulation. 2000 Jul 25;102(4):432-7. doi: 10.1161/01.cir.102.4.432. Circulation. 2000. PMID: 10908216

8

Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms.

Minelli A, Capra E, Dellavecchia C, Danesino C, Olivieri C, Tateo S, Tenti P, Scappaticci S. Minelli A, et al. Among authors: dellavecchia c. Eur J Gynaecol Oncol. 1998;19(3):234-8. Eur J Gynaecol Oncol. 1998. PMID: 9641220

9

Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.

Danesino C, Pasquali F, Dellavecchia C, Maserati E, Minelli A, Seghezzi L. Danesino C, et al. Among authors: dellavecchia c. Am J Med Genet. 1998 Dec 28;80(5):540. doi: 10.1002/(sici)1096-8628(19981228)80:5<540::aid-ajmg25>3.0.co;2-8. Am J Med Genet. 1998. PMID: 9880228 No abstract available.

10

The breakpoints of a constitutional inversion of chromosome 9 associated with haemophagocytic lymphohistiocytosis are not linked to the disease gene.

Aricò M, Dellavecchia C, Piantanida M, Clementi R, Hasle H, Conter V, D'Angelo P, Varotto S, Santoro N, Danesino C. Aricò M, et al. Among authors: dellavecchia c. Br J Haematol. 1999 Jan;104(1):108-10. doi: 10.1046/j.1365-2141.1999.01151.x. Br J Haematol. 1999. PMID: 10027721 Free article.

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