Publications by authors named "F Mugneret"

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Isolated isochromosomes i(X)(p10) and idic(X)(q13) are associated with myeloid malignancies and dysplastic features.
Dominique Penther, Pascaline Etancelin, Daniel Lusina, Audrey Bidet, Benoit Quilichini, Francine Mugneret

Am J Hematol· November 2019

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Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?
S El Chehadeh, R Touraine, F Prieur, W Reardon, T Bienvenu, F Mugneret

Clin Genet· April 2017

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NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis.
S Struski, S Lagarde, P Bories, C Puiseux, N Prade, F Mugneret

Leukemia· March 2017

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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study.
Nicolas Gruchy, Eleonore Blondeel, Nathalie Le Meur, Géraldine Joly-Hélas, Pascal Chambon, Francine Mugneret

Prenat Diagn· June 2016

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Genetic differences between paediatric and adult Burkitt lymphomas.
Violaine Havelange, Xavier Pepermans, Geneviève Ameye, Ivan Théate, Evelyne Callet-Bauchu, Francine Mugneret

Br J Haematol· April 2016

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