Works matching AU Jamar, Mauricette

Results: 12

Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 1, p. 35, doi. 10.1002/gepi.22019

By:

Wenric, Stephane;
Sticca, Tiberio;
Caberg, Jean‐Hubert;
Josse, Claire;
Fasquelle, Corinne;
Herens, Christian;
Jamar, Mauricette;
Max, Stéphanie;
Gothot, André;
Caers, Jo;
Bours, Vincent

Publication type:

Article

Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 1, p. 1, doi. 10.1038/sj.ejhg.5200575

By:

Verloes, Alain;
Gillerot, Yves;
Van Maldergem, Lionel;
Schoos, Roland;
Herens, Christian;
Jamar, Mauricette;
Dideberg, Vinciane;
Lesenfants, Sylviane;
Koulischer, Lucien

Publication type:

Article

CHIC cells: a novel ALK+ cell line derived from a relapsed anaplastic large cell lymphoma.

Published in:

British Journal of Haematology, 2011, v. 152, n. 3, p. 356, doi. 10.1111/j.1365-2141.2010.08414.x

By:

Thielen, Caroline;
Bisig, Bettina;
Gofflot, Stéphanie;
Herens, Christian;
Fillet, Georges;
Jamar, Mauricette;
Tassin, Françoise;
Boniver, Jacques;
Drion, Pierre;
de Leval, Laurence

Publication type:

Article

Prenatally detected copy number variants in a national cohort: A postnatal follow‐up study.

Published in:

Prenatal Diagnosis, 2020, v. 40, n. 10, p. 1272, doi. 10.1002/pd.5751

By:

Muys, Joke;
Jacquemyn, Yves;
Blaumeiser, Bettina;
Bourlard, Laura;
Brison, Nathalie;
Bulk, Saskia;
Chiarappa, Patrizia;
De Leener, Anne;
De Rademaeker, Marjan;
Désir, Julie;
Destrée, Anne;
Devriendt, Koenraad;
Dheedene, Annelies;
Duquenne, Armelle;
Fieuw, Annelies;
Fransen, Erik;
Gatot, Jean‐Stéphane;
Jamar, Mauricette;
Janssens, Sandra;
Kerstjens, Jorien

Publication type:

Article

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.

Published in:

2018

By:

Muys, Joke;
Blaumeiser, Bettina;
Jacquemyn, Yves;
Bandelier, Claude;
Brison, Nathalie;
Bulk, Saskia;
Chiarappa, Patrizia;
Courtens, Winnie;
De Leener, Anne;
De Rademaeker, Marjan;
Désir, Julie;
Destrée, Anne;
Devriendt, Koenraad;
Dheedene, Annelies;
Fieuw, Annelies;
Fransen, Erik;
Gatot, Jean‐Stéphane;
Holmgren, Philip;
Jamar, Mauricette;
Janssens, Sandra

Publication type:

journal article

Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.

Published in:

2016

By:

Uwineza, Annette;
Hitayezu, Janvier;
Jamar, Mauricette;
Caberg, Jean-Hubert;
Murorunkwere, Seraphine;
Janvier, Ndinkabandi;
Bours, Vincent;
Mutesa, Leon

Publication type:

journal article

Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity.

Published in:

Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 18, doi. 10.1002/gcc.22397

By:

Sticca, Tiberio;
Caberg, Jean‐Hubert;
Wenric, Stephane;
Poulet, Christophe;
Herens, Christian;
Jamar, Mauricette;
Josse, Claire;
El Guendi, Sonia;
Max, Stéphanie;
Beguin, Yves;
Gothot, André;
Caers, Jo;
Bours, Vincent

Publication type:

Article

Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin-2 stimulation: A Belgian multicentric study.

Published in:

Genes, Chromosomes & Cancer, 2009, v. 48, n. 10, p. 843, doi. 10.1002/gcc.20691

By:

Put, Natalie;
Konings, Peter;
Rack, Katrina;
Jamar, Mauricette;
Roy, Nadine Van;
Libouton, Jeanne-Marie;
Vannuffel, Pascal;
Sartenaer, Daniel;
Ameye, Geneviève;
Speleman, Frank;
Herens, Christian;
Poirel, Hélène A.;
Moreau, Yves;
Hagemeijer, Anne;
Vandenberghe, Peter;
Michaux, Lucienne

Publication type:

Article

Pattern of congenital heart diseases in Rwandan children with genetic defects.

Published in:

Pan African Medical Journal, 2014, v. 19, p. 1, doi. 10.11604/pamj.2014.19.85.3428

By:

Teteli, Raissa;
Uwineza, Annette;
Butera, Yvan;
Hitayezu, Janvier;
Murorunkwere, Seraphine;
Umurerwa, Lamberte;
Ndinkabandi, Janvier;
Hellin, Anne-Cécile;
Jamar, Mauricette;
Caberg, Jean-Hubert;
Muganga, Narcisse;
Mucumbitsi, Joseph;
Rusingiza, Emmanuel Kamanzi;
Mutesa, Leon

Publication type:

Article

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

Published in:

Human Genetics, 2001, v. 109, n. 3, p. 286, doi. 10.1007/s004390100585

By:

Riegel, Mariluce;
Baumer, Alessandra;
Jamar, Mauricette;
Delbecque, Kathy;
Herens, Christian;
Verloes, Alain;
Schinzel, Albert

Publication type:

Article

Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study.

Published in:

Annals of Hematology, 2012, v. 91, n. 2, p. 203, doi. 10.1007/s00277-011-1286-0

By:

Mullier, François;
Daliphard, Sylvie;
Garand, Richard;
Dekeyser, Mélanie;
Cornet, Yvan;
Luquet, Isabelle;
Talmant, Pascaline;
Richebourg, Steven;
Jamar, Mauricette;
Dogné, Jean-Michel;
Chatelain, Christian;
Michaux, Lucienne;
Chatelain, Bernard

Publication type:

Article

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.

Published in:

BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-79

By:

Uwineza, Annette;
Caberg, Jean-Hubert;
Hitayezu, Janvier;
Hellin, Anne Cecile;
Jamar, Mauricette;
Dideberg, Vinciane;
Rusingiza, Emmanuel K.;
Bours, Vincent;
Mutesa, Leon

Publication type:

Article