Publications by authors named "D Fauvert"

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A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.
M Ben Khelifa, F Ghieh, R Boudjenah, C Hue, D Fauvert

Hum Reprod· June 2018

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First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.
Sarah Guterman, Bérénice Hervé, Julie Rivière, Delphine Fauvert, Patrice Clement

J Obstet Gynaecol Res· March 2018

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The emerging microduplication 3q13.31: Expanding the genotype-phenotype correlations of the reciprocal microdeletion 3q13.31 syndrome.
B Hervé, D Fauvert, R Dard, J Roume, S Cognard

Eur J Med Genet· September 2016

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Low-level mosaicism of a de novo derivative chromosome 9 from a t(5;9)(q35.1;q34.3) has a major phenotypic impact.
B Hervé, J Roume, S Cognard, D Fauvert, D Molina-Gomes

Eur J Med Genet· March 2016

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15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Delphine Fauvert

Eur J Med Genet· March 2015

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