Capon F - Search Results

1

Mapping a dominant form of multinodular goiter to chromosome Xp22.

Capon F, Tacconelli A, Giardina E, Sciacchitano S, Bruno R, Tassi V, Trischitta V, Filetti S, Dallapiccola B, Novelli G. Capon F, et al. Am J Hum Genet. 2000 Oct;67(4):1004-7. doi: 10.1086/303095. Epub 2000 Sep 11. Am J Hum Genet. 2000. PMID: 10986044 Free PMC article.

2

Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11.

Salehi LB, Mangino M, De Serio S, De Cicco D, Capon F, Semprini S, Pizzuti A, Novelli G, Dallapiccola B. Salehi LB, et al. Among authors: capon f. Hum Genet. 2002 Oct;111(4-5):401-4. doi: 10.1007/s00439-002-0785-4. Epub 2002 Aug 21. Hum Genet. 2002. PMID: 12384783

3

Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22.

Mangino M, Sanchez O, Torrente I, De Luca A, Capon F, Novelli G, Dallapiccola B. Mangino M, et al. Among authors: capon f. Am J Hum Genet. 1999 Aug;65(2):441-7. doi: 10.1086/302505. Am J Hum Genet. 1999. PMID: 10417287 Free PMC article.

4

Advances in the search for psoriasis susceptibility genes.

Capon F, Dallapiccola B, Novelli G. Capon F, et al. Mol Genet Metab. 2000 Sep-Oct;71(1-2):250-5. doi: 10.1006/mgme.2000.3031. Mol Genet Metab. 2000. PMID: 11001818 Review.

5

Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.

Sangiuolo F, Bruscia E, Capon F, Servidei S, Dallapiccola B, Novelli G. Sangiuolo F, et al. Among authors: capon f. Eur J Hum Genet. 2000 Oct;8(10):809-12. doi: 10.1038/sj.ejhg.5200547. Eur J Hum Genet. 2000. PMID: 11039585

6

Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.

Mangino M, Flex E, Capon F, Sangiuolo F, Carraro E, Gualandi F, Mazzoli M, Martini A, Novelli G, Dallapiccola B. Mangino M, et al. Among authors: capon f. Eur J Hum Genet. 2001 Sep;9(9):667-71. doi: 10.1038/sj.ejhg.5200707. Eur J Hum Genet. 2001. PMID: 11571554

7

Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees.

Semprini S, Capon F, Tacconelli A, Giardina E, Orecchia A, Mingarelli R, Gobello T, Zambruno G, Botta A, Fabrizi G, Novelli G. Semprini S, et al. Among authors: capon f. Hum Genet. 2002 Oct;111(4-5):310-3. doi: 10.1007/s00439-002-0812-5. Epub 2002 Aug 21. Hum Genet. 2002. PMID: 12384771

8

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C.

Novelli G, Muchir A, Sangiuolo F, Helbling-Leclerc A, D'Apice MR, Massart C, Capon F, Sbraccia P, Federici M, Lauro R, Tudisco C, Pallotta R, Scarano G, Dallapiccola B, Merlini L, Bonne G. Novelli G, et al. Among authors: capon f. Am J Hum Genet. 2002 Aug;71(2):426-31. doi: 10.1086/341908. Epub 2002 Jun 19. Am J Hum Genet. 2002. PMID: 12075506 Free PMC article.

9

Mutational analysis of Peroxiredoxin IV: exclusion of a positional candidate for multinodular goitre.

Giardina E, Capon F, D'Apice MR, Amati F, Arturi F, Filetti S, Bonifazi E, Pucci S, Conte C, Novelli G. Giardina E, et al. Among authors: capon f. BMC Med Genet. 2002 Jul 23;3:5. doi: 10.1186/1471-2350-3-5. Epub 2002 Jul 23. BMC Med Genet. 2002. PMID: 12135533 Free PMC article.

10

PCR protocol for DNA recovery from Spurr's-embedded muscle biopsies.

Capon F, Cicero SL, Novelli G, Dallapiccola B. Capon F, et al. PCR Methods Appl. 1993 Dec;3(3):211-2. doi: 10.1101/gr.3.3.211. PCR Methods Appl. 1993. PMID: 8118405 Free article. No abstract available.

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