Vekemans M - Search Results

1

Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features.

Fert-Ferrer S, Guichet A, Tantau J, Delezoide AL, Ozilou C, Romana SP, Gosset P, Viot G, Loison S, Moraine C, Morichon-Delvallez N, Turleau C, Vekemans M, Prieur M. Fert-Ferrer S, et al. Among authors: vekemans m. Prenat Diagn. 2000 Jun;20(6):511-5. doi: 10.1002/1097-0223(200006)20:6<511::aid-pd849>3.0.co;2-b. Prenat Diagn. 2000. PMID: 10861719

2

Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature.

Malan V, Martinovic J, Sanlaville D, Caillat S, Waill MC, Ganne ML, Tantau J, Attie-Bitach T, Vekemans M, Morichon-Delvallez N. Malan V, et al. Among authors: vekemans m. Prenat Diagn. 2006 Mar;26(3):231-8. doi: 10.1002/pd.1386. Prenat Diagn. 2006. PMID: 16450350 Review.

3

Prenatal diagnosis and characterization of an analphoid marker chromosome 16.

Tabet AC, Gosset P, Elghezal H, Fontaine S, Martinovic J, Encha Razavi F, Romana S, Vekemans M, Morichon-Delvallez N. Tabet AC, et al. Among authors: vekemans m. Prenat Diagn. 2004 Sep;24(9):733-6. doi: 10.1002/pd.804. Prenat Diagn. 2004. PMID: 15386469

4

Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature.

Faivre L, Morichon-Delvallez N, Viot G, Narcy F, Loison S, Mandelbrot L, Aubry MC, Raclin V, Edery P, Munnich A, Vekemans M. Faivre L, et al. Among authors: vekemans m. Prenat Diagn. 1998 Oct;18(10):1055-60. doi: 10.1002/(sici)1097-0223(1998100)18:10<1055::aid-pd405>3.0.co;2-i. Prenat Diagn. 1998. PMID: 9826897 Review.

5

Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature.

Faivre L, Morichon-Delvallez N, Viot G, Martinovic J, Pinson MP, Aubry JP, Raclin V, Edery P, Dumez Y, Munnich A, Vekemans M. Faivre L, et al. Among authors: vekemans m. Prenat Diagn. 1999 Jan;19(1):49-53. Prenat Diagn. 1999. PMID: 10073907 Review.

6

Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.

Faivre L, Morichon-Delvallez N, Viot G, Larget-Piet A, Narcy F, Turleau C, Pinson MP, Dumez Y, Munnich A, Vekemans M. Faivre L, et al. Among authors: vekemans m. Prenat Diagn. 1999 Mar;19(3):282-6. Prenat Diagn. 1999. PMID: 10210132 Review.

7

Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.

Faivre L, Gosset P, Cormier-Daire V, Odent S, Amiel J, Giurgea I, Nassogne MC, Pasquier L, Munnich A, Romana S, Prieur M, Vekemans M, De Blois MC, Turleau C. Faivre L, et al. Among authors: vekemans m. Eur J Hum Genet. 2002 Nov;10(11):699-706. doi: 10.1038/sj.ejhg.5200879. Eur J Hum Genet. 2002. PMID: 12404101

8

Molecular screening of the ZFHX1B gene in prenatally diagnosed isolated agenesis of the corpus callosum.

Espinosa-Parrilla Y, Encha-Razavi F, Attié-Bitach T, Martinovic J, Morichon-Delvallez N, Munnich A, Vekemans M, Lyonnet S, Amiel J. Espinosa-Parrilla Y, et al. Among authors: vekemans m. Prenat Diagn. 2004 Apr;24(4):298-301. doi: 10.1002/pd.865. Prenat Diagn. 2004. PMID: 15065106

9

Functional disomy of the Xq28 chromosome region.

Sanlaville D, Prieur M, de Blois MC, Genevieve D, Lapierre JM, Ozilou C, Picq M, Gosset P, Morichon-Delvallez N, Munnich A, Cormier-Daire V, Baujat G, Romana S, Vekemans M, Turleau C. Sanlaville D, et al. Among authors: vekemans m. Eur J Hum Genet. 2005 May;13(5):579-85. doi: 10.1038/sj.ejhg.5201384. Eur J Hum Genet. 2005. PMID: 15741994 Review.

10

[New developments in cytogenetics].

Turleau C, Vekemans M. Turleau C, et al. Among authors: vekemans m. Med Sci (Paris). 2005 Nov;21(11):940-6. doi: 10.1051/medsci/20052111940. Med Sci (Paris). 2005. PMID: 16274645 Free article. Review. French.

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