Devoto M - Search Results

1

Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation.

Mirghomizadeh F, Bardtke B, Devoto M, Pfister M, Oeken J, König E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N. Mirghomizadeh F, et al. Among authors: devoto m. Eur J Hum Genet. 2002 Feb;10(2):95-9. doi: 10.1038/sj.ejhg.5200769. Eur J Hum Genet. 2002. PMID: 11938438

2

A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.

Pfister M, Thiele H, Van Camp G, Fransen E, Apaydin F, Aydin O, Leistenschneider P, Devoto M, Zenner HP, Blin N, Nürnberg P, Ozkarakas H, Kupka S. Pfister M, et al. Among authors: devoto m. Cell Physiol Biochem. 2004;14(4-6):369-76. doi: 10.1159/000080347. Cell Physiol Biochem. 2004. PMID: 15319541

3

Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12.

Vitale E, Cook S, Sun R, Specchia C, Subramanian K, Rocchi M, Nathanson D, Schwalb M, Devoto M, Rohowsky-Kochan C. Vitale E, et al. Among authors: devoto m. Hum Mol Genet. 2002 Feb 1;11(3):295-300. doi: 10.1093/hmg/11.3.295. Hum Mol Genet. 2002. PMID: 11823448

4

Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p.

Vitale E, Brancolini V, De Rienzo A, Bird L, Allada V, Sklansky M, Chae CU, Ferrero GB, Weber J, Devoto M, Casey B. Vitale E, et al. Among authors: devoto m. J Med Genet. 2001 Mar;38(3):182-5. doi: 10.1136/jmg.38.3.182. J Med Genet. 2001. PMID: 11303511 Free PMC article. No abstract available.

5

Homogeneity of cystic fibrosis in Italy.

Vitale E, Devoto M, Mastella G, Romeo G. Vitale E, et al. Among authors: devoto m. Am J Hum Genet. 1986 Dec;39(6):832-6. Am J Hum Genet. 1986. PMID: 3467589 Free PMC article.

6

Novel X-linked mental retardation syndrome with short stature maps to Xq24.

Vitale E, Specchia C, Devoto M, Angius A, Rong S, Rocchi M, Schwalb M, Demelas L, Paglietti D, Manca S, Mastropaolo C, Serra G. Vitale E, et al. Among authors: devoto m. Am J Med Genet. 2001 Sep 15;103(1):1-8. doi: 10.1002/ajmg.1495. Am J Med Genet. 2001. PMID: 11562927

7

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

Petrukhin K, Fischer SG, Pirastu M, Tanzi RE, Chernov I, Devoto M, Brzustowicz LM, Cayanis E, Vitale E, Russo JJ, et al. Petrukhin K, et al. Among authors: devoto m. Nat Genet. 1993 Dec;5(4):338-43. doi: 10.1038/ng1293-338. Nat Genet. 1993. PMID: 8298640

8

A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24.

Deglincerti A, De Giorgio R, Cefle K, Devoto M, Pippucci T, Castegnaro G, Panza E, Barbara G, Cogliandro RF, Mungan Z, Palanduz S, Corinaldesi R, Romeo G, Seri M, Stanghellini V. Deglincerti A, et al. Among authors: devoto m. Eur J Hum Genet. 2007 Aug;15(8):889-97. doi: 10.1038/sj.ejhg.5201844. Epub 2007 May 9. Eur J Hum Genet. 2007. PMID: 17487221

9

Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets.

Bolino A, Devoto M, Enia G, Zoccali C, Weissenbach J, Romeo G. Bolino A, et al. Among authors: devoto m. Eur J Hum Genet. 1993;1(4):269-79. doi: 10.1159/000472424. Eur J Hum Genet. 1993. PMID: 7915957

10

Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.

Annese V, Latiano A, Bovio P, Forabosco P, Piepoli A, Lombardi G, Andreoli A, Astegiano M, Gionchetti P, Riegler G, Sturniolo GC, Clementi M, Rappaport E, Fortina P, Devoto M, Gasparini P, Andriulli A. Annese V, et al. Among authors: devoto m. Eur J Hum Genet. 1999 Jul;7(5):567-73. doi: 10.1038/sj.ejhg.5200328. Eur J Hum Genet. 1999. PMID: 10439963

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