Publications by authors named "M Jamar"

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Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Mauricette Jamar

Prenat Diagn· September 2020

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The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Mauricette Jamar

Prenat Diagn· December 2018

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Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity.
Tiberio Sticca, Jean-Hubert Caberg, Stephane Wenric, Christophe Poulet, Christian Herens, Mauricette Jamar

Genes Chromosomes Cancer· January 2017

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Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample.
Stephane Wenric, Tiberio Sticca, Jean-Hubert Caberg, Claire Josse, Corinne Fasquelle, Mauricette Jamar

Genet Epidemiol· January 2017

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Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.
Annette Uwineza, Janvier Hitayezu, Mauricette Jamar, Jean-Hubert Caberg, Seraphine Murorunkwere

J Trop Pediatr· February 2016

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