Giollant M - Search Results

1

A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask-like facial syndrome.

Debost-Legrand A, Eymard-Pierre E, Pebrel-Richard C, Gouas L, Goumy C, Giollant M, Ayed W, Tchirkov A, Francannet C, Vago P. Debost-Legrand A, et al. Among authors: giollant m. Am J Med Genet A. 2013 Jan;161A(1):162-5. doi: 10.1002/ajmg.a.35614. Epub 2012 Dec 13. Am J Med Genet A. 2013. PMID: 23239647

2

Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature review.

Blanc P, Gouas L, Francannet C, Giollant M, Vago P, Goumy C. Blanc P, et al. Among authors: giollant m. Am J Med Genet A. 2008 May 15;146A(10):1307-11. doi: 10.1002/ajmg.a.32278. Am J Med Genet A. 2008. PMID: 18384146 Review.

3

Familial deletion 11q14.3-q22.1 without apparent phenotypic consequences: a haplosufficient 8.5 Mb region.

Goumy C, Gouas L, Tchirkov A, Roucaute T, Giollant M, Veronèse L, Francannet C, Vago P. Goumy C, et al. Among authors: giollant m. Am J Med Genet A. 2008 Oct 15;146A(20):2668-72. doi: 10.1002/ajmg.a.32511. Am J Med Genet A. 2008. PMID: 18798310

4

An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis.

Goumy C, Mihaescu M, Tchirkov A, Giollant M, Bonnet-Dupeyron MN, Jaffray JY, Geneix A, Perissel B, Francannet C, Boespflug-Tanguy O, Vago P. Goumy C, et al. Among authors: giollant m. Morphologie. 2005 Jun;89(285):71-5. doi: 10.1016/s1286-0115(05)83241-2. Morphologie. 2005. PMID: 16110742

5

De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.

Goumy C, Mihaescu M, Tchirkov A, Giollant M, Benier C, Francannet C, Jaffray JY, Geneix A, Vago P. Goumy C, et al. Among authors: giollant m. Genet Couns. 2006;17(3):371-9. Genet Couns. 2006. PMID: 17100206

6

Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p.

Goumy C, Beaufrère AM, Tchirkov A, Gouas L, Gaspard F, Giollant M, Roucaute T, Veronèse L, Lemery D, Vago P. Goumy C, et al. Among authors: giollant m. Prenat Diagn. 2008 Feb;28(2):131-4. doi: 10.1002/pd.1928. Prenat Diagn. 2008. PMID: 18236428

7

[From "monocolor" karyotype to "multicolor" karyotype: applications of M-Fish in hematology and oncology].

Jaffray JY, Giollant M, Perissel B, Vago P. Jaffray JY, et al. Among authors: giollant m. Bull Cancer. 2002 Feb;89(2):174-80. Bull Cancer. 2002. PMID: 11888857 Free article. Review. French.

8

Cytogenetic characterization of seven human cancer cell lines by combining G- and R-banding, M-FISH, CGH and chromosome- and locus-specific FISH.

Cottier M, Tchirkov A, Perissel B, Giollant M, Campos L, Vago P. Cottier M, et al. Among authors: giollant m. Int J Mol Med. 2004 Oct;14(4):483-95. Int J Mol Med. 2004. PMID: 15375617

9

Characterization of double minute chromosomes' DNA content in a human high grade astrocytoma cell line by using comparative genomic hybridization and fluorescence in situ hybridization.

Giollant M, Bertrand S, Verrelle P, Tchirkov A, du Manoir S, Ried T, Mornex F, Doré JF, Cremer T, Malet P. Giollant M, et al. Hum Genet. 1996 Sep;98(3):265-70. doi: 10.1007/s004390050205. Hum Genet. 1996. PMID: 8707292

10

Detection of heterozygous carriers of the ataxia-telangiectasia (ATM) gene by G2 phase chromosomal radiosensitivity of peripheral blood lymphocytes.

Tchirkov A, Bay JO, Pernin D, Bignon YJ, Rio P, Grancho M, Kwiatkowski F, Giollant M, Malet P, Verrelle P. Tchirkov A, et al. Among authors: giollant m. Hum Genet. 1997 Dec;101(3):312-6. doi: 10.1007/s004390050634. Hum Genet. 1997. PMID: 9439660

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