Morel F - Search Results

1

Prenatal diagnosis of mosaic tetrasomy 8p.

Le Bris MJ, Marcorelles P, Audrézet MP, Parent P, Heren P, Le Guern H, Herry A, Morel F, Collet M, Férec C, De Braekeleer M. Le Bris MJ, et al. Among authors: morel f. Am J Med Genet A. 2003 Jul 1;120A(1):44-8. doi: 10.1002/ajmg.a.20199. Am J Med Genet A. 2003. PMID: 12794691

2

Familial interstitial deletion of the short arm of chromosome 4 (p15.33-p16.3) characterized by molecular cytogenetic analysis.

Basinko A, Douet-Guilbert N, Parent P, Blondin G, Mingam M, Monot F, Morel F, Le Bris MJ, De Braekeleer M. Basinko A, et al. Among authors: morel f. Am J Med Genet A. 2008 Apr 1;146A(7):899-903. doi: 10.1002/ajmg.a.32138. Am J Med Genet A. 2008. PMID: 18302281

3

Molecular cytogenetic characterization of an 8p22-8p23.2 duplication derived from a maternal intrachromosomal insertion in a child with congenital heart malformation, delayed puberty, and learning disabilities.

Basinko A, Douet-Guilbert N, Le Bris MJ, Parent P, Ansquer H, Morel F, De Braekeleer M. Basinko A, et al. Among authors: morel f. Am J Med Genet A. 2008 Nov 15;146A(22):2950-4. doi: 10.1002/ajmg.a.32522. Am J Med Genet A. 2008. PMID: 18924175 No abstract available.

4

Characterization and meiotic segregation of a supernumerary marker chromosome in sperm of infertile males: case report and literature review.

Perrin A, Nguyen MH, Delobel B, Guéganic N, Basinko A, Le Bris MJ, Douet-Guilbert N, De Braekeleer M, Morel F. Perrin A, et al. Among authors: morel f. Eur J Med Genet. 2012 Dec;55(12):743-6. doi: 10.1016/j.ejmg.2012.09.004. Epub 2012 Sep 20. Eur J Med Genet. 2012. PMID: 23000562 Review.

5

Molecular cytogenetic characterization of two small chromosome 8 derived supernumerary mosaic markers.

Herry A, Morel F, Le Bris MJ, Bellec V, Lallaoui H, Parent P, De Braekeleer M. Herry A, et al. Among authors: morel f. Am J Med Genet A. 2004 Jul 1;128A(1):33-8. doi: 10.1002/ajmg.a.30077. Am J Med Genet A. 2004. PMID: 15211653

6

Detection of an unexpected subtelomeric 15q26.2 --> qter deletion in a little girl: clinical and cytogenetic studies.

Pinson L, Perrin A, Plouzennec C, Parent P, Metz C, Collet M, Le Bris MJ, Douet-Guilbert N, Morel F, De Braekeleer M. Pinson L, et al. Among authors: morel f. Am J Med Genet A. 2005 Oct 1;138A(2):160-5. doi: 10.1002/ajmg.a.30939. Am J Med Genet A. 2005. PMID: 16114049 Review.

7

Prenatal diagnosis of a mosaic 45,X/46,X,r(X)46,XX with a small ring of the X chromosome.

Le Bris MJ, Le Guern H, Plouhinec C, Audrezet MP, Parent P, Chabaud JJ, Morel F, De Braekeleer M, Douet-Guilbert N. Le Bris MJ, et al. Among authors: morel f. Genet Couns. 2006;17(4):429-34. Genet Couns. 2006. PMID: 17375529

8

18p trisomy: a case of direct 18p duplication characterized by molecular cytogenetic analysis.

Marical H, Le Bris MJ, Douet-Guilbert N, Parent P, Descourt JP, Morel F, De Braekeleer M. Marical H, et al. Among authors: morel f. Am J Med Genet A. 2007 Sep 15;143A(18):2192-5. doi: 10.1002/ajmg.a.31881. Am J Med Genet A. 2007. PMID: 17676610 No abstract available.

9

AML1 amplification in a case of childhood acute lymphoblastic leukemia.

Morel F, Herry A, Le Bris MJ, Douet-Guilbert N, Le Calvez G, Marion V, Berthou C, De Braekeeler M. Morel F, et al. Cancer Genet Cytogenet. 2002 Sep;137(2):142-5. doi: 10.1016/s0165-4608(02)00566-6. Cancer Genet Cytogenet. 2002. PMID: 12393286

10

Trisomy 15 as the sole abnormality in myelodysplastic syndromes: case report and review of the literature.

Morel F, Le Bris MJ, Herry A, Morice P, De Braekeleer M. Morel F, et al. Leuk Lymphoma. 2003 Mar;44(3):549-51. doi: 10.1080/1042819021000055084. Leuk Lymphoma. 2003. PMID: 12688332 Review.

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