Doco-Fenzy M - Search Results

1

Pure direct duplication (12)(q24.1-->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies.

Doco-Fenzy M, Mauran P, Lebrun JM, Bock S, Bednarek N, Struski S, Albuisson J, Ardalan A, Collot N, Schneider A, Dastot-Le Moal F, Gaillard D, Goossens M. Doco-Fenzy M, et al. Am J Med Genet A. 2006 Feb 1;140(3):212-21. doi: 10.1002/ajmg.a.31057. Am J Med Genet A. 2006. PMID: 16411218

2

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.

Maillard AM, Ruef A, Pizzagalli F, Migliavacca E, Hippolyte L, Adaszewski S, Dukart J, Ferrari C, Conus P, Männik K, Zazhytska M, Siffredi V, Maeder P, Kutalik Z, Kherif F, Hadjikhani N, Beckmann JS, Reymond A, Draganski B, Jacquemont S; 16p11.2 European Consortium. Maillard AM, et al. Mol Psychiatry. 2015 Feb;20(1):140-7. doi: 10.1038/mp.2014.145. Epub 2014 Nov 25. Mol Psychiatry. 2015. PMID: 25421402 Free PMC article.

3

Use of chromosome painting for marker chromosome identification in two children with congenital disorders.

Doco-Fenzy M, Navrocki B, Cornillet P, Sabouraud P, Robillard P, Gruson N, Gaillard D, Adnet JJ. Doco-Fenzy M, et al. Bull Assoc Anat (Nancy). 1994 Jun;78(241):9-13. Bull Assoc Anat (Nancy). 1994. PMID: 8086666

4

Investigation of nonimmune hydrops fetalis: multidisciplinary studies are necessary for diagnosis--review of 94 cases.

Lallemand AV, Doco-Fenzy M, Gaillard DA. Lallemand AV, et al. Pediatr Dev Pathol. 1999 Sep-Oct;2(5):432-9. doi: 10.1007/s100249900146. Pediatr Dev Pathol. 1999. PMID: 10441620

5

Identification of chromosomal loci associated with non-P-glycoprotein-mediated multidrug resistance to topoisomerase II inhibitor in lung adenocarcinoma cell line by comparative genomic hybridization.

Struski S, Doco-Fenzy M, Trussardi A, Masson L, Gruson N, Ulrich E, Proult M, Jardillier JC, Potron G, Cornillet-Lefebvre P. Struski S, et al. Genes Chromosomes Cancer. 2001 Feb;30(2):136-42. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1071>3.0.co;2-t. Genes Chromosomes Cancer. 2001. PMID: 11135430

6

Cytogenetic characterization of chromosomal rearrangement in a human vinblastine-resistant CEM cell line: use of comparative genomic hybridization and fluorescence in situ hybridization.

Struski S, Cornillet-Lefebvre P, Doco-Fenzy M, Dufer J, Ulrich E, Masson L, Michel N, Gruson N, Potron G. Struski S, et al. Cancer Genet Cytogenet. 2002 Jan 1;132(1):51-4. doi: 10.1016/s0165-4608(01)00519-2. Cancer Genet Cytogenet. 2002. PMID: 11801309

7

Compilation of published comparative genomic hybridization studies.

Struski S, Doco-Fenzy M, Cornillet-Lefebvre P. Struski S, et al. Cancer Genet Cytogenet. 2002 May;135(1):63-90. doi: 10.1016/s0165-4608(01)00624-0. Cancer Genet Cytogenet. 2002. PMID: 12072205 Review.

8

Cytogenetic evolution of human ovarian cell lines associated with chemoresistance and loss of tumorigenicity.

Struski S, Doco-Fenzy M, Koehler M, Chudoba I, Levy F, Masson L, Michel N, Ulrich E, Gruson N, Bénard J, Potron G, Cornillet-Lefebvre P. Struski S, et al. Anal Cell Pathol. 2003;25(3):115-22. doi: 10.1155/2003/151042. Anal Cell Pathol. 2003. PMID: 12775915 Free PMC article.

9

Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia.

Schneider A, Benzacken B, Guichet A, Verloes A, Bonneau D, Collot N, Dastot-Le-Moal F, Goossens M, Taine L, Landais E, Gaillard D, Doco-Fenzy M. Schneider A, et al. Eur J Hum Genet. 2008 Jun;16(6):680-7. doi: 10.1038/sj.ejhg.5201977. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197200

10

The clinical spectrum associated with a chromosome 17 short arm proximal duplication (dup 17p11.2) in three patients.

Doco-Fenzy M, Holder-Espinasse M, Bieth E, Magdelaine C, Vincent MC, Khoury M, Andrieux J, Zhang F, Lupski JR, Klink R, Schneider A, Goze-Martineau O, Cuisset JM, Vallee L, Manouvrier-Hanu S, Gaillard D, de Martinville B. Doco-Fenzy M, et al. Am J Med Genet A. 2008 Apr 1;146A(7):917-24. doi: 10.1002/ajmg.a.32195. Am J Med Genet A. 2008. PMID: 18327785

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