Publications by authors named "Agnes Choiset"

5Publications

A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH.

Authors:
Céline Poirsier Justine Besseau-Ayasse Caroline Schluth-Bolard Jérôme Toutain Chantal Missirian Cédric Le Caignec Anne Bazin Marie Christine de Blois Paul Kuentz Marie Catty Agnès Choiset Ghislaine Plessis Audrey Basinko Pascaline Letard Elisabeth Flori Mélanie Jimenez Mylène Valduga Emilie Landais Hakima Lallaoui François Cartault James Lespinasse Dominique Martin-Coignard Patrick Callier Céline Pebrel-Richard Marie-France Portnoi Tiffany Busa Aline Receveur Florence Amblard Catherine Yardin Radu Harbuz Fabienne Prieur Nathalie Le Meur Eva Pipiras Pascale Kleinfinger François Vialard Martine Doco-Fenzy

Eur J Hum Genet 2016 06 28;24(6):844-51. Epub 2015 Oct 28.

Département de Génétique, CHU de Reims, Reims, France.

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June 2016

Pattern of secretion of pregnancy-associated plasma protein-A (PAPP-A) during pregnancies complicated by fetal aneuploidy, in vivo and in vitro.

Authors:
Marie Clémence Leguy Stephanie Brun Guillaume Pidoux Houria Salhi Agnes Choiset Marie Claude Menet Sophie Gil Vassilis Tsatsaris Jean Guibourdenche

Reprod Biol Endocrinol 2014 Dec 28;12:129. Epub 2014 Dec 28.

Hormonology CHU Cochin AP-HP, 27 rue du Fbg St Jacques, Paris, France.

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December 2014

Amniocentesis performed for karyotyping after identified ultrasonographic abnormalities: what to expect?

Authors:
Patrice Gaudry Maxime Esvan Jean-Baptiste Meynard Aziza Lebbar Agnès Choiset Fanny Lewin Vassili Tsatsaris Emmanuelle Pannier Gilles Grange

Fetal Diagn Ther 2012 13;31(1):55-62. Epub 2011 Dec 13.

Department of Obstetrics and Gynecology, Hôpital d'Instruction des Armées Begin, Saint-Mandé, France.

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November 2012

Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: an array-CGH study.

Authors:
Aurélie Coussement Philippe Lochu Jean-Michel Dupont Agnès Choiset

Am J Med Genet A 2011 Oct 9;155A(10):2597-600. Epub 2011 Sep 9.

Laboratoire de Cytogénétique, Groupe Hospitalier Cochin-Saint Vincent de Paul, AP-HP, Paris, France.

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October 2011

Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20.

Authors:
Azarnouche Ardalan Marguerite Prieur Agnès Choiset Catherine Turleau Françoise Goutieres Sylvie Girard-Orgeolet

Am J Med Genet A 2005 Oct;138A(3):288-93

Laboratoire de Cytogénétique, Groupe Hospitalier Cochin-Saint-Vincent-de-Paul, Paris, France.

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October 2005