Publications by authors named "Marguerite Prieur"

6Publications

Paraoxonase-1 expression is up-regulated in Down syndrome fetal liver.

Authors:
Nathalie Janel Olivier Christophe Emilie Aït Yahya-Graison Julien Hamelet Evelyne Paly Marguerite Prieur Anne-Lise Delezoïde Jean Maurice Delabar

Biochem Biophys Res Commun 2006 Aug 16;346(4):1303-6. Epub 2006 Jun 16.

EA 3508, Université Paris 7--Denis Diderot, Paris, France.

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August 2006

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

Failure to detect an 8p22-8p23.1 duplication in patients with Kabuki (Niikawa-Kuroki) syndrome.

Authors:
Damien Sanlaville David Genevieve Céline Bernardin Jeanne Amiel Clarisse Baumann Marie-Christine de Blois Valérie Cormier-Daire Bénédicte Gerard Marion Gerard Martine Le Merrer Philippe Parent Fabienne Prieur Marguerite Prieur Odile Raoul Annick Toutain Alain Verloes Géraldine Viot Serge Romana Arnold Munnich Stanislas Lyonnet Michel Vekemans Catherine Turleau

Eur J Hum Genet 2005 May;13(5):690-3

Département de Génétique, Hôpital Necker Enfants Malades, Paris, France.

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May 2005

Functional disomy of the Xq28 chromosome region.

Authors:
Damien Sanlaville Marguerite Prieur Marie-Christine de Blois David Genevieve Jean-Michel Lapierre Catherine Ozilou Monique Picq Philippe Gosset Nicole Morichon-Delvallez Arnold Munnich Valerie Cormier-Daire Genevieve Baujat Serge Romana Michel Vekemans Catherine Turleau

Eur J Hum Genet 2005 May;13(5):579-85

Département de Génétique, Hôpital Necker-Enfants Malades, Paris, France.

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May 2005

Parathyroid function and growth in 22q11.2 deletion syndrome.

Authors:
Raja Brauner Agnes Le Harivel de Gonneville Catherine Kindermans Jérone Le Bidois Marguerite Prieur Stanislaus Lyonnet Jean-Claude Souberbielle

J Pediatr 2003 May;142(5):504-8

Université René Descartes and Pediatric Endocrinology Unit, Fondation-Hôpital Saint Joseph, Paris, France.

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May 2003

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

Authors:
Laurence Faivre Philippe Gosset Valérie Cormier-Daire Sylvie Odent Jeanne Amiel Irina Giurgea Marie-Cécile Nassogne Laurent Pasquier Arnold Munnich Serge Romana Marguerite Prieur Michel Vekemans Marie-Christine De Blois Catherine Turleau

Eur J Hum Genet 2002 Nov;10(11):699-706

Département de Génétique, Hôpital Necker-Enfants Malades, Paris, France.

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November 2002