Grosso M - Search Results

1

Prenatal diagnosis of cystic fibrosis: a case of twin pregnancy diagnosis and a review of 5 years' experience.

Castaldo G, Martinelli P, Massa C, Fuccio A, Grosso M, Rippa E, Paladini D, Salvatore F. Castaldo G, et al. Among authors: grosso m. Clin Chim Acta. 2000 Aug;298(1-2):121-33. doi: 10.1016/s0009-8981(00)00284-9. Clin Chim Acta. 2000. PMID: 10876009 Review.

2

Molecular genetic characterization and prenatal diagnosis in a family with Hunter disease.

Grosso M, Balzano N, Rippa E, Villani GR, Salvatore F, Izzo P, di Natale P. Grosso M, et al. Biochem Mol Biol Int. 1995 May;35(6):1261-7. Biochem Mol Biol Int. 1995. PMID: 7492964

3

A unique origin for Sicilian (delta beta) (0)-thalassemia in 33 unrelated families and its rapid diagnostic characterization by PCR analysis.

Esposito G, Grosso M, Gottardi E, Izzo P, Camaschella C, Salvatore F. Esposito G, et al. Among authors: grosso m. Hum Genet. 1994 Jun;93(6):691-3. doi: 10.1007/BF00201572. Hum Genet. 1994. PMID: 8005594

4

Multiple control elements regulate transcription from the most distal promoter of human aldolase A gene.

Costanzo P, Lupo A, Rippa E, Grosso M, Salvatore F, Izzo P. Costanzo P, et al. Among authors: grosso m. Biochem Biophys Res Commun. 1993 Sep 15;195(2):935-44. doi: 10.1006/bbrc.1993.2134. Biochem Biophys Res Commun. 1993. PMID: 8373426

5

Mucopolysaccharidosis type II: identification of six novel mutations in Italian patients.

Villani GR, Balzano N, Grosso M, Salvatore F, Izzo P, Di Natale P. Villani GR, et al. Among authors: grosso m. Hum Mutat. 1997;10(1):71-5. doi: 10.1002/(SICI)1098-1004(1997)10:1<71::AID-HUMU10>3.0.CO;2-X. Hum Mutat. 1997. PMID: 9222763 No abstract available.

6

Frequency distribution of mitochondrial DNA haplogroups in Corsica and Sardinia.

Morelli L, Grosso MG, Vona G, Varesi L, Torroni A, Francalacci P. Morelli L, et al. Among authors: grosso mg. Hum Biol. 2000 Aug;72(4):585-95. Hum Biol. 2000. PMID: 11048788

7

Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects.

Duraturo F, Liccardo R, Cavallo A, De Rosa M, Grosso M, Izzo P. Duraturo F, et al. Among authors: grosso m. Int J Cancer. 2011 Oct 1;129(7):1643-50. doi: 10.1002/ijc.25824. Epub 2011 Apr 25. Int J Cancer. 2011. PMID: 21128252

8

Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases.

Grosso M, Puzone S, Storino MR, Sessa R, Izzo P. Grosso M, et al. Clin Chem Lab Med. 2013 Dec;51(12):2219-25. doi: 10.1515/cclm-2013-0195. Clin Chem Lab Med. 2013. PMID: 23612661

9

[Mutation analysis in Hunter patients].

Villani GR, Balzano N, Grosso M, Di Natale P. Villani GR, et al. Among authors: grosso m. Pediatr Med Chir. 1996 Jan-Feb;18(1):71-83. Pediatr Med Chir. 1996. PMID: 8685029 Review. Italian.

10

Detection of four novel mutations in the iduronate-2-sulfatase gene. Mutations in brief no. 123. Online.

Balzano N, Villani GR, Grosso M, Izzo P, Di Natale P. Balzano N, et al. Among authors: grosso m. Hum Mutat. 1998;11(4):333. doi: 10.1002/(SICI)1098-1004(1998)11:4<333::AID-HUMU18>3.0.CO;2-G. Hum Mutat. 1998. PMID: 10215411

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