Pierluigi M - 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: pierluigi m. 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: pierluigi m. 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. Among authors: pierluigi m. Am J Med Genet Suppl. 1990;7:141-7. doi: 10.1002/ajmg.1320370729. Am J Med Genet Suppl. 1990. PMID: 1981474

4

An improved method for the detection of Down's syndrome aneuploidy in uncultured amniocytes.

Pierluigi M, Perfumo C, Cavani S, Lehrach H, Nizetic D, Dagna Bricarelli FD. Pierluigi M, et al. Clin Genet. 1996 Jan;49(1):32-6. doi: 10.1111/j.1399-0004.1996.tb04321.x. Clin Genet. 1996. PMID: 8721569

5

Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.

Pierluigi M, Battaglia P, Perfumo C, Baroncini A, Bricarelli FD. Pierluigi M, et al. Ann Genet. 1997;40(2):99-103. Ann Genet. 1997. PMID: 9259956

6

Effect of x-rays on chromosome 21 nondisjunction.

Strigini P, Pierluigi M, Forni GL, Sansone R, Carobbi S, Grasso M, Dagna Bricarelli F. Strigini P, et al. Among authors: pierluigi m. Am J Med Genet Suppl. 1990;7:155-9. doi: 10.1002/ajmg.1320370731. Am J Med Genet Suppl. 1990. PMID: 2149939

7

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: pierluigi m. Hum Genet. 1989 Dec;84(1):63-5. doi: 10.1007/BF00210673. Hum Genet. 1989. PMID: 2532615

8

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: pierluigi m. Hum Genet. 1988 Jun;79(2):124-7. doi: 10.1007/BF00280549. Hum Genet. 1988. PMID: 2899052

9

[In situ ++hybridization with painting probes in the definition of reciprocal translocations].

Pierluigi M, Perfumo C, Arslanian A, Giannotti A, Dagna Bricarelli F. Pierluigi M, et al. Pathologica. 1994 Feb;86(1):106-9. Pathologica. 1994. PMID: 8072796 Italian.

10

Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations.

Cavani S, Perfumo C, Faravelli F, Malacarne M, Sogliani M, Piombo G, Zerega G, Zucca M, Dagna Bricarelli F, Pierluigi M. Cavani S, et al. Among authors: pierluigi m. Prenat Diagn. 2003 Oct;23(10):819-23. doi: 10.1002/pd.678. Prenat Diagn. 2003. PMID: 14558026

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