Morichon-Delvallez N - Search Results

1

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. Prenat Diagn. 1999 Jan;19(1):49-53. Prenat Diagn. 1999. PMID: 10073907 Review.

2

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. Prenat Diagn. 2004 Apr;24(4):298-301. doi: 10.1002/pd.865. Prenat Diagn. 2004. PMID: 15065106

3

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: morichon delvallez n. Prenat Diagn. 2006 Mar;26(3):231-8. doi: 10.1002/pd.1386. Prenat Diagn. 2006. PMID: 16450350 Review.

4

Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia.

Quenum-Miraillet G, Malan V, Martinovic J, Encha-Razavi F, Aral B, Texier I, Bonnefont JP, Vekemans M, Morichon-Delvallez N. Quenum-Miraillet G, et al. Among authors: morichon delvallez n. Prenat Diagn. 2008 Jan;28(1):69-71. doi: 10.1002/pd.1911. Prenat Diagn. 2008. PMID: 18186139 No abstract available.

5

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. 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.

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. Prenat Diagn. 1999 Mar;19(3):282-6. Prenat Diagn. 1999. PMID: 10210132 Review.

7

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. 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

8

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. Prenat Diagn. 2004 Sep;24(9):733-6. doi: 10.1002/pd.804. Prenat Diagn. 2004. PMID: 15386469

9

Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy.

Golzio C, Guirchoun J, Ozilou C, Thomas S, Goudefroye G, Morichon-Delvallez N, Vekemans M, Attié-Bitach T, Etchevers HC. Golzio C, et al. Among authors: morichon delvallez n. Prenat Diagn. 2006 Dec;26(13):1201-5. doi: 10.1002/pd.1588. Prenat Diagn. 2006. PMID: 17075794

10

Duplication of the long arm of chromosome 13 secondary to a recombination in a maternal intrachromosomal insertion (shift).

Vekemans M, Morichon-Delvallez N. Vekemans M, et al. Prenat Diagn. 1990 Dec;10(12):787-94. doi: 10.1002/pd.1970101205. Prenat Diagn. 1990. PMID: 1963687 Review.

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