Levanat S - Search Results

1

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.

Shimkets R, Gailani MR, Siu VM, Yang-Feng T, Pressman CL, Levanat S, Goldstein A, Dean M, Bale AE. Shimkets R, et al. Among authors: levanat s. Am J Hum Genet. 1996 Aug;59(2):417-22. Am J Hum Genet. 1996. PMID: 8755929 Free PMC article.

2

A two-hit model for developmental defects in Gorlin syndrome.

Levanat S, Gorlin RJ, Fallet S, Johnson DR, Fantasia JE, Bale AE. Levanat S, et al. Nat Genet. 1996 Jan;12(1):85-7. doi: 10.1038/ng0196-85. Nat Genet. 1996. PMID: 8528259 No abstract available.

3

Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region.

Levanat S, Chidambaram A, Wicking C, Bray-Ward P, Pressman C, Toftgard R, Gailani MR, Myers JC, Wainwright B, Dean M, Bale AE. Levanat S, et al. Cytogenet Cell Genet. 1997;76(3-4):208-13. doi: 10.1159/000134551. Cytogenet Cell Genet. 1997. PMID: 9186526

4

Direct molecular analysis of archival tumor tissue for loss of heterozygosity.

Johnson DR, Levanat S, Bale AE. Johnson DR, et al. Among authors: levanat s. Biotechniques. 1995 Aug;19(2):190-2. Biotechniques. 1995. PMID: 8527133 No abstract available.

5

Clinical utility gene card for: Gorlin syndrome.

Lo Muzio L, Pastorino L, Levanat S, Musani V, Situm M, Scarra GB. Lo Muzio L, et al. Among authors: levanat s. Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.9. Epub 2011 Feb 9. Eur J Hum Genet. 2011. PMID: 21304560 Free PMC article. No abstract available.

6

Clinical utility gene card for: Gorlin syndrome--update 2013.

Lo Muzio L, Pastorino L, Levanat S, Musani V, Situm M, Ponti G, Bianchi Scarra G. Lo Muzio L, et al. Among authors: levanat s. Eur J Hum Genet. 2013 Oct;21(10). doi: 10.1038/ejhg.2012.299. Epub 2013 Jan 30. Eur J Hum Genet. 2013. PMID: 23361221 Free PMC article. No abstract available.

7

Variable expression of Gorlin syndrome may reflect complexity of the signalling pathway.

Levanat S, Mubrin MK, Crnić I, Situm M, Basta-Juzbasić A. Levanat S, et al. Pflugers Arch. 2000;439(3 Suppl):R31-3. Pflugers Arch. 2000. PMID: 10653132

8

Involvement of patched (PTCH) gene in Gorlin syndrome and related disorders: three family cases.

Situm M, Levanat S, Crnic I, Pavelic B, Macan D, Grgurević J, Mubrin-Koncar M, Lipozencić J. Situm M, et al. Among authors: levanat s. Croat Med J. 1999 Dec;40(4):533-8. Croat Med J. 1999. PMID: 10554356 Free article.

9

Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.

Musani V, Ozretić P, Trnski D, Sabol M, Poduje S, Tošić M, Šitum M, Levanat S. Musani V, et al. Among authors: levanat s. Croat Med J. 2018 Feb 28;59(1):20-24. doi: 10.3325/cmj.2018.59.20. Croat Med J. 2018. PMID: 29498494 Free PMC article.

10

Gorlin syndrome patient with large deletion in 9q22.32-q22.33 detected by quantitative multiplex fluorescent PCR.

Musani V, Cretnik M, Situm M, Basta-Juzbasic A, Levanat S. Musani V, et al. Among authors: levanat s. Dermatology. 2009;219(2):111-8. doi: 10.1159/000219247. Epub 2009 May 14. Dermatology. 2009. PMID: 19439922 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

64 results

Search Page

Filters