Miozzo M - Search Results

1

Three cases with de novo 6q imbalance and variable prenatal phenotype.

Grati FR, Lalatta F, Turolla L, Cavallari U, Gentilin B, Rossella F, Cetin I, Antonazzo P, Bellotti M, Dulcetti F, Baldo D, Tenconi R, Simoni G, Miozzo M. Grati FR, et al. Among authors: miozzo m. Am J Med Genet A. 2005 Jul 30;136(3):254-8. doi: 10.1002/ajmg.a.30837. Am J Med Genet A. 2005. PMID: 15957159

2

Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression.

Miozzo M, Grati FR, Bulfamante G, Rossella F, Cribiù M, Radaelli T, Cassani B, Persico T, Cetin I, Pardi G, Simoni G. Miozzo M, et al. Placenta. 2001 Nov;22(10):813-21. doi: 10.1053/plac.2001.0728. Placenta. 2001. PMID: 11718568

3

The role of imprinted genes in fetal growth.

Miozzo M, Simoni G. Miozzo M, et al. Biol Neonate. 2002;81(4):217-28. doi: 10.1159/000056752. Biol Neonate. 2002. PMID: 12011565 Review.

4

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.

Grati FR, Sirchia SM, Gentilin B, Rossella F, Ramoscelli L, Antonazzo P, Cavallari U, Bulfamante G, Cetin I, Simoni G, Miozzo M. Grati FR, et al. Among authors: miozzo m. Eur J Hum Genet. 2004 Apr;12(4):272-8. doi: 10.1038/sj.ejhg.5201121. Eur J Hum Genet. 2004. PMID: 14673477

5

Frequency of monosomy X in women with primary biliary cirrhosis.

Invernizzi P, Miozzo M, Battezzati PM, Bianchi I, Grati FR, Simoni G, Selmi C, Watnik M, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: miozzo m. Lancet. 2004 Feb 14;363(9408):533-5. doi: 10.1016/S0140-6736(04)15541-4. Lancet. 2004. PMID: 14975617

6

Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.

Ruggeri A, Dulcetti F, Miozzo M, Grati FR, Grimi B, Bellato S, Natacci F, Maggi F, Simoni G. Ruggeri A, et al. Among authors: miozzo m. Prenat Diagn. 2004 Dec 15;24(12):997-1000. doi: 10.1002/pd.961. Prenat Diagn. 2004. PMID: 15614836

7

Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies.

Grati FR, Miozzo M, Cassani B, Rossella F, Antonazzo P, Gentilin B, Sirchia SM, Mori L, Rigano S, Bulfamante G, Cetin I, Simoni G. Grati FR, et al. Among authors: miozzo m. Placenta. 2005 Jan;26(1):10-8. doi: 10.1016/j.placenta.2004.04.009. Placenta. 2005. PMID: 15664406

8

Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells.

Sirchia SM, Ramoscelli L, Grati FR, Barbera F, Coradini D, Rossella F, Porta G, Lesma E, Ruggeri A, Radice P, Simoni G, Miozzo M. Sirchia SM, et al. Among authors: miozzo m. Cancer Res. 2005 Mar 15;65(6):2139-46. doi: 10.1158/0008-5472.CAN-04-3465. Cancer Res. 2005. PMID: 15781624 Free article.

9

X chromosome monosomy: a common mechanism for autoimmune diseases.

Invernizzi P, Miozzo M, Selmi C, Persani L, Battezzati PM, Zuin M, Lucchi S, Meroni PL, Marasini B, Zeni S, Watnik M, Grati FR, Simoni G, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: miozzo m. J Immunol. 2005 Jul 1;175(1):575-8. doi: 10.4049/jimmunol.175.1.575. J Immunol. 2005. PMID: 15972694

10

Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.

Grati FR, Grimi B, Frascoli G, Di Meco AM, Liuti R, Milani S, Trotta A, Dulcetti F, Grosso E, Miozzo M, Maggi F, Simoni G. Grati FR, et al. Among authors: miozzo m. Eur J Hum Genet. 2006 Mar;14(3):282-8. doi: 10.1038/sj.ejhg.5201564. Eur J Hum Genet. 2006. PMID: 16418738

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