Perroni L - Search Results

1

Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21q.

Cavani S, Perfumo C, Argusti A, Pierluigi M, Perroni L, Schmiegelow K, Petersen MB, Cotter FE, Strigini P, Dagna-Bricarelli F, Nizetić D. Cavani S, et al. Among authors: perroni l. Br J Haematol. 1998 Oct;103(1):213-6. doi: 10.1046/j.1365-2141.1998.00924.x. Br J Haematol. 1998. PMID: 9792310 Free article.

2

Origin of extra chromosome 21 in 343 families: cytogenetic and molecular approaches.

Dagna Bricarelli F, Pierluigi M, Grasso M, Strigini P, Perroni L. Dagna Bricarelli F, et al. Among authors: perroni l. Am J Med Genet Suppl. 1990;7:129-32. doi: 10.1002/ajmg.1320370726. Am J Med Genet Suppl. 1990. PMID: 1981472

3

Crossing over and chromosome 21 nondisjunction: a study of 60 families.

Perroni L, Dagna Bricarelli F, Grasso M, Pierluigi M, Baldi M, Pedemonte C, Strigini P. Perroni L, et al. Am J Med Genet Suppl. 1990;7:141-7. doi: 10.1002/ajmg.1320370729. Am J Med Genet Suppl. 1990. PMID: 1981474

4

Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: a study of 87 families.

Perroni L, Grasso M, Argusti A, Lo Nigro C, Croci GF, Zelante L, Garani GP, Dagna Bricarelli F. Perroni L, et al. Am J Med Genet. 1996 Jul 12;64(1):176-80. doi: 10.1002/(SICI)1096-8628(19960712)64:1<176::AID-AJMG30>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8826470

5

Isochromosome not translocation in trisomy 21q21q.

Grasso M, Giovannucci Uzielli ML, Pierluigi M, Tavellini F, Perroni L, Dagna Bricarelli F. Grasso M, et al. Among authors: perroni l. Hum Genet. 1989 Dec;84(1):63-5. doi: 10.1007/BF00210673. Hum Genet. 1989. PMID: 2532615

6

High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms.

Bricarelli FD, Pierluigi M, Perroni L, Grasso M, Arslanian A, Sacchi N. Bricarelli FD, et al. Among authors: perroni l. Hum Genet. 1988 Jun;79(2):124-7. doi: 10.1007/BF00280549. Hum Genet. 1988. PMID: 2899052

7

Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome.

Grasso M, Perroni L, Colella S, Piombo G, Argusti A, Lituania M, Buscaglia M, Giussani U, Grimoldi MG, Bricarelli FD. Grasso M, et al. Among authors: perroni l. Am J Med Genet. 1996 Jul 12;64(1):187-90. doi: 10.1002/(SICI)1096-8628(19960712)64:1<187::AID-AJMG33>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8826473

8

Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: III. Molecular analysis with the StB12.3 probe.

Grasso M, Perroni L, Dagna-Bricarelli F, Rinaldi A, Robledo R, Siniscalco M, Filippi G. Grasso M, et al. Among authors: perroni l. Am J Med Genet. 1996 Aug 9;64(2):283-6. doi: 10.1002/(SICI)1096-8628(19960809)64:2<283::AID-AJMG10>3.0.CO;2-B. Am J Med Genet. 1996. PMID: 8844066

9

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.

Grasso M, Faravelli F, Lo Nigro C, Chiurazzi P, Sperandeo MP, Argusti A, Pomponi MG, Lecora M, Sebastio GF, Perroni L, Andria G, Neri G, Bricarelli FD. Grasso M, et al. Among authors: perroni l. Am J Med Genet. 1999 Jul 30;85(3):311-6. doi: 10.1002/(sici)1096-8628(19990730)85:3<311::aid-ajmg24>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10398249

10

FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.

Lo Nigro C, Faravelli F, Cavani S, Perroni L, Novello P, Vitali M, Bricarelli FD, Grasso M. Lo Nigro C, et al. Among authors: perroni l. Eur J Hum Genet. 2000 Mar;8(3):157-62. doi: 10.1038/sj.ejhg.5200425. Eur J Hum Genet. 2000. PMID: 10780779

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