Maud Favier

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 10

Top Topics

Clinical Practice

Human Immunodeficiency Virus

Top Venues

Prenatal diagnosis

This page only lists publications with an associated author ORCID identifier.

Publications

Pierre-Louis Forey, Maud Favier, Claire Beneteau, Sophie Berenguer, Lydie Da Costa, Virginie Guigue, Philippe Loget, Julia Torrents, Laura Samaison, Didier Riethmuller, Sophie Collardeau-Frachon
Acute fetal leukemia: When should it be suspected? What assessment should be performed? A case series and review of literature. Prenatal diagnosis (2024)
Maud Favier, Rodolph Dard, Guillaume Gorincour, Aude Tessier, Emmanuelle Motte-Signoret, Clemence Duvillier, Caroline Racine, Laurence Faivre, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencing. Prenatal diagnosis (2024)
Maud Favier, Julian Delanne, Guillaume Gorincour, Laurence Faivre, Caroline Racine, Christophe Philippe, Yannis Duffourd, Antonio Vitobello, Thierry Rousseau, Olivia Martz, Georges Tarris, Camélia Oualiken, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not? Prenatal diagnosis 44 (3) (2024)
Maud Favier, Julian Delanne, Guillaume Gorincour, Laurence Faivre, Caroline Racine, Christophe Philippe, Yannis Duffourd, Antonio Vitobello, Thierry Rousseau, Olivia Martz, Georges Tarris, Camélia Oualiken, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not? Prenatal diagnosis 44 (3) (2024)
Maud Favier, Rodolph Dard, Guillaume Gorincour, Aude Tessier, Emmanuelle Motte-Signoret, Clemence Duvillier, Caroline Racine, Laurence Faivre, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencing. Prenatal diagnosis 44 (9) (2024)
Maud Favier, Rodolph Dard, Guillaume Gorincour, Aude Tessier, Emmanuelle Motte-Signoret, Clemence Duvillier, Caroline Racine, Laurence Faivre, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencing. Prenatal diagnosis 44 (9) (2024)
Maud Favier, Julian Delanne, Guillaume Gorincour, Laurence Faivre, Caroline Racine, Christophe Philippe, Yannis Duffourd, Antonio Vitobello, Thierry Rousseau, Olivia Martz, Georges Tarris, Camélia Oualiken, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not? Prenatal diagnosis (2024)
Maud Favier, Rodolph Dard, Guillaume Gorincour, Aude Tessier, Emmanuelle Motte-Signoret, Clemence Duvillier, Caroline Racine, Laurence Faivre, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencing. Prenatal diagnosis 44 (9) (2024)
Maud Favier, Rodolph Dard, Guillaume Gorincour, Aude Tessier, Emmanuelle Motte-Signoret, Clemence Duvillier, Caroline Racine, Laurence Faivre, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencing. Prenatal diagnosis 44 (9) (2024)
Maud Favier, Julian Delanne, Guillaume Gorincour, Laurence Faivre, Caroline Racine, Christophe Philippe, Yannis Duffourd, Antonio Vitobello, Thierry Rousseau, Olivia Martz, Georges Tarris, Camélia Oualiken, Christel Thauvin-Robinet, Frédéric Tran Mau Them
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not? Prenatal diagnosis 44 (3) (2024)