Patrosso MC - Search Results

1

Fidelity of a YAC clone in the region of human MCF-2 gene.

Patrosso MC, Frattini A, Susani L, Vezzoni P, Villa A. Patrosso MC, et al. Biochem Biophys Res Commun. 1991 Dec 16;181(2):877-83. doi: 10.1016/0006-291x(91)91272-e. Biochem Biophys Res Commun. 1991. PMID: 1684496

2

Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28.

Frattini A, Faranda S, Redolfi E, Zucchi I, Villa A, Patrosso MC, Strina D, Susani L, Vezzoni P. Frattini A, et al. Among authors: patrosso mc. Genomics. 1994 Sep 1;23(1):30-5. doi: 10.1006/geno.1994.1455. Genomics. 1994. PMID: 7829097

3

A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.

Ferlini A, Patrosso MC, Repetto M, Frattini A, Villa A, Fini S, Salvi F, Vezzoni P, Forabosco A. Ferlini A, et al. Among authors: patrosso mc. Hum Mutat. 1994;4(1):61-4. doi: 10.1002/humu.1380040110. Hum Mutat. 1994. PMID: 7951260 No abstract available.

4

The exon-intron organization of the human X-linked gene (FLN1) encoding actin-binding protein 280.

Patrosso MC, Repetto M, Villa A, Milanesi L, Frattini A, Faranda S, Mancini M, Maestrini E, Toniolo D, Vezzoni P. Patrosso MC, et al. Genomics. 1994 May 1;21(1):71-6. doi: 10.1006/geno.1994.1226. Genomics. 1994. PMID: 8088819

5

Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders.

Ferlini A, Patrosso MC, Guidetti D, Merlini L, Uncini A, Ragno M, Plasmati R, Fini S, Repetto M, Vezzoni P, et al. Ferlini A, et al. Among authors: patrosso mc. Am J Med Genet. 1995 Jan 2;55(1):105-11. doi: 10.1002/ajmg.1320550125. Am J Med Genet. 1995. PMID: 7702080

6

C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by hyper IgM syndrome.

Villa A, Strina D, Macchi P, Patrosso MC, Vezzoni P, Tovo PA, Giliani S, Ugazio AG, Notarangelo LD. Villa A, et al. Among authors: patrosso mc. Hum Mutat. 1994;3(1):73-5. doi: 10.1002/humu.1380030115. Hum Mutat. 1994. PMID: 7906987 No abstract available.

7

Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosis.

Ferlini A, Fini S, Salvi F, Patrosso MC, Vezzoni P, Forabosco A. Ferlini A, et al. Among authors: patrosso mc. FASEB J. 1992 Jul;6(10):2864-6. doi: 10.1096/fasebj.6.10.1353040. FASEB J. 1992. PMID: 1353040

8

X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene.

Villa A, Notarangelo L, Macchi P, Mantuano E, Cavagni G, Brugnoni D, Strina D, Patrosso MC, Ramenghi U, Sacco MG, et al. Villa A, et al. Among authors: patrosso mc. Nat Genet. 1995 Apr;9(4):414-7. doi: 10.1038/ng0495-414. Nat Genet. 1995. PMID: 7795648

9

Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis.

Patrosso MC, Salvi F, De Grandis D, Vezzoni P, Jacobson DR, Ferlini A. Patrosso MC, et al. Am J Med Genet. 1998 May 1;77(2):135-8. doi: 10.1002/(sici)1096-8628(19980501)77:2<135::aid-ajmg5>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9605286

10

Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings.

Ferlini A, Salvi F, Uncini A, el-Chami J, Winter P, Altland K, Repetto M, Littardi M, Campoleoni A, Vezzoni P, Patrosso MC. Ferlini A, et al. Among authors: patrosso mc. Clin Genet. 1996 Jan;49(1):10-4. doi: 10.1111/j.1399-0004.1996.tb04317.x. Clin Genet. 1996. PMID: 8721565

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