Mignon-Ravix C - Search Results

1

Intrachromosomal triplication for the distal part of chromosome 15q.

Schluth C, Mattei MG, Mignon-Ravix C, Salman S, Alembik Y, Willig J, Ginglinger E, Jeandidier E. Schluth C, et al. Am J Med Genet A. 2005 Jul 15;136(2):179-84. doi: 10.1002/ajmg.a.30745. Am J Med Genet A. 2005. PMID: 15940678 Review.

2

Maternally inherited duplication of the possible imprinted 14q31 region.

Mignon-Ravix C, Mugneret F, Stavropoulou C, Depetris D, Khau Van Kien P, Mattei MG. Mignon-Ravix C, et al. J Med Genet. 2001 May;38(5):343-7. doi: 10.1136/jmg.38.5.343. J Med Genet. 2001. PMID: 11403046 Free PMC article. No abstract available.

3

A human interstitial telomere associates in vivo with specific TRF2 and TIN2 proteins.

Mignon-Ravix C, Depetris D, Delobel B, Croquette MF, Mattei MG. Mignon-Ravix C, et al. Eur J Hum Genet. 2002 Feb;10(2):107-12. doi: 10.1038/sj.ejhg.5200775. Eur J Hum Genet. 2002. PMID: 11938440

4

Mechanism of intrachromosomal triplications 15q11-q13: a new clinical report.

Vialard F, Mignon-Ravix C, Parain D, Depetris D, Portnoï MF, Moirot H, Mattei MG. Vialard F, et al. Am J Med Genet A. 2003 Apr 30;118A(3):229-34. doi: 10.1002/ajmg.a.10164. Am J Med Genet A. 2003. PMID: 12673652

5

Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.

Luciani JJ, de Mas P, Depetris D, Mignon-Ravix C, Bottani A, Prieur M, Jonveaux P, Philippe A, Bourrouillou G, de Martinville B, Delobel B, Vallee L, Croquette MF, Mattei MG. Luciani JJ, et al. J Med Genet. 2003 Sep;40(9):690-6. doi: 10.1136/jmg.40.9.690. J Med Genet. 2003. PMID: 12960216 Free PMC article. No abstract available.

6

Subcellular distribution of HP1 proteins is altered in ICF syndrome.

Luciani JJ, Depetris D, Missirian C, Mignon-Ravix C, Metzler-Guillemain C, Megarbane A, Moncla A, Mattei MG. Luciani JJ, et al. Eur J Hum Genet. 2005 Jan;13(1):41-51. doi: 10.1038/sj.ejhg.5201293. Eur J Hum Genet. 2005. PMID: 15470359

7

Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.

Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG. Mignon-Ravix C, et al. Eur J Hum Genet. 2007 Apr;15(4):432-40. doi: 10.1038/sj.ejhg.5201775. Epub 2007 Jan 31. Eur J Hum Genet. 2007. PMID: 17264869

8

In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin.

Metzler-Guillemain C, Depetris D, Luciani JJ, Mignon-Ravix C, Mitchell MJ, Mattei MG. Metzler-Guillemain C, et al. Chromosome Res. 2008;16(5):761-82. doi: 10.1007/s10577-008-1225-7. Epub 2008 Jul 4. Chromosome Res. 2008. PMID: 18592385

9

PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase.

Luciani JJ, Depetris D, Usson Y, Metzler-Guillemain C, Mignon-Ravix C, Mitchell MJ, Megarbane A, Sarda P, Sirma H, Moncla A, Feunteun J, Mattei MG. Luciani JJ, et al. J Cell Sci. 2006 Jun 15;119(Pt 12):2518-31. doi: 10.1242/jcs.02965. Epub 2006 May 30. J Cell Sci. 2006. PMID: 16735446

10

Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.

Haddad MR, Mignon-Ravix C, Cacciagli P, Mégarbané A, Villard L. Haddad MR, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):211-7. doi: 10.1016/j.ejmg.2009.04.002. Epub 2009 Apr 18. Eur J Med Genet. 2009. PMID: 19379847

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

30 results

Search Page

Filters