Chessa L - Search Results

1

The phenotype of partial dup(7q) reconsidered: a report of five new cases.

Forabosco A, Baroncini A, Dalpra L, Chessa L, Giannotti A, Maccagnani F, Dallapiccola B. Forabosco A, et al. Among authors: chessa l. Clin Genet. 1988 Jul;34(1):48-59. doi: 10.1111/j.1399-0004.1988.tb02615.x. Clin Genet. 1988. PMID: 3409538

2

Translocation Y/5 resulting in Cri du Chat syndrome.

Vignetti P, Chessa L, Bruni L, Ferrante E, Dallapiccola B. Vignetti P, et al. Among authors: chessa l. Clin Genet. 1977 Dec;12(6):319-22. doi: 10.1111/j.1399-0004.1977.tb00949.x. Clin Genet. 1977. PMID: 589854

3

Mating between two balanced translocation carriers in two unrelated families.

Dallapiccola B, Chessa L, Brinchi V, Frontali M, Gandini E. Dallapiccola B, et al. Among authors: chessa l. Hum Genet. 1983;65(2):165-8. doi: 10.1007/BF00286655. Hum Genet. 1983. PMID: 6654331

4

Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).

Dallapiccola B, Chessa L, Vignetti P, Ferrante E, Gandini E. Dallapiccola B, et al. Among authors: chessa l. Hum Genet. 1979;50(1):45-9. doi: 10.1007/BF00295588. Hum Genet. 1979. PMID: 468260

5

Segregation of an X ring chromosome in two generations.

Dallapiccola B, Bruni L, Boscherini B, Pasquino AM, Chessa L, Vignetti P. Dallapiccola B, et al. Among authors: chessa l. J Med Genet. 1980 Aug;17(4):306-8. doi: 10.1136/jmg.17.4.306. J Med Genet. 1980. PMID: 7205906 Free PMC article.

6

[Trisomy 10p due to t(Y;10)(p11; p11) "de novo"].

Chessa L, Vignetti P, Ferrante E, Dallapiccola B. Chessa L, et al. Pathologica. 1979 May-Jun;71(1013):353-4. Pathologica. 1979. PMID: 548875 Italian. No abstract available.

7

[A case of pure, clear, "de novo" trisomy 9p].

Vignetti P, Bruni L, Ferrante E, Chessa L, Dallapiccola B. Vignetti P, et al. Among authors: chessa l. Pathologica. 1979 May-Jun;71(1013):349. Pathologica. 1979. PMID: 548873 Italian. No abstract available.

8

Chromosome studies in patients with T-CLL chronic lymphocytic leukemia and expansions of granular lymphocytes.

Dallapiccola B, Alimena G, Chessa L, Gastaldi R, De Rossi G, Semenzato G, Quinti I, Pandolfi F. Dallapiccola B, et al. Among authors: chessa l. Int J Cancer. 1984 Aug 15;34(2):171-6. doi: 10.1002/ijc.2910340206. Int J Cancer. 1984. PMID: 6332081

9

Founder effects for ATM gene mutations in Italian Ataxia Telangiectasia families.

Chessa L, Piane M, Magliozzi M, Torrente I, Savio C, Lulli P, De Luca A, Dallapiccola B. Chessa L, et al. Ann Hum Genet. 2009 Sep;73(Pt 5):532-9. doi: 10.1111/j.1469-1809.2009.00535.x. Ann Hum Genet. 2009. PMID: 19691550

10

Heterogeneity in ataxia-telangiectasia: classical phenotype associated with intermediate cellular radiosensitivity.

Chessa L, Petrinelli P, Antonelli A, Fiorilli M, Elli R, Marcucci L, Federico A, Gandini E. Chessa L, et al. Am J Med Genet. 1992 Mar 1;42(5):741-6. doi: 10.1002/ajmg.1320420524. Am J Med Genet. 1992. PMID: 1632451 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

225 results

Search Page

Filters