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JAMAR, Mauricette
33  results:
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1

Prenatally detected copy number variants in a national coho..:

Muys, Joke ; Jacquemyn, Yves ; Blaumeiser, Bettina...
Prenatal Diagnosis.  40 (2020)  10 - p. 1272-1283 , 2020
Link: https://doi.org/10.1002/..
 
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2

The Belgian MicroArray Prenatal (BEMAPRE) database: A syste..:

Muys, Joke ; Blaumeiser, Bettina ; Jacquemyn, Yves...
Prenatal Diagnosis.  38 (2018)  13 - p. 1120-1128 , 2018
Link: https://doi.org/10.1002/..
 
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3

Exome copy number variation detection: Use of a pool of unr..:

Wenric, Stephane ; Sticca, Tiberio ; Caberg, Jean-Hubert...
Genetic Epidemiology.  41 (2016)  1 - p. 35-40 , 2016
Link: https://doi.org/10.1002/..
 
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4

Genomic studies of multiple myeloma reveal an association b..:

Sticca, Tiberio ; Caberg, Jean‐Hubert ; Wenric, Stephane...
Genes, Chromosomes and Cancer.  56 (2016)  1 - p. 18-27 , 2016
Link: https://doi.org/10.1002/..
 
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5

Cytogenetic Studies of Rwandan Pediatric Patients Presentin..:

Uwineza, Annette ; Hitayezu, Janvier ; Jamar, Mauricette...
Journal of Tropical Pediatrics.  62 (2015)  1 - p. 38-45 , 2015
Link: https://doi.org/10.1093/..
 
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6

Pattern of congenital heart diseases in Rwandan children wi..:

Teteli, Raissa ; Uwineza, Annette ; Butera, Yvan...
Pan African Medical Journal.  19 (2014)  - p. , 2014
Link: https://doi.org/10.11604..
 
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7

Array-CGH analysis in Rwandan patients presenting developme..:

Uwineza, Annette ; Caberg, Jean-Hubert ; Hitayezu, Janvier...
BMC Medical Genetics.  15 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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8

Morphology, cytogenetics, and survival in myelodysplasia wi..:

Mullier, François ; Daliphard, Sylvie ; Garand, Richard...
Annals of Hematology.  91 (2011)  2 - p. 203-213 , 2011
Link: https://doi.org/10.1007/..
 
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9

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

Thielen, Caroline ; Bisig, Bettina ; Gofflot, Stéphanie...
British Journal of Haematology.  152 (2010)  3 - p. 356-360 , 2010
Link: https://doi.org/10.1111/..
 
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10

Improved detection of chromosomal abnormalities in chronic ..:

Put, Natalie ; Konings, Peter ; Rack, Katrina...
Genes, Chromosomes and Cancer.  48 (2009)  10 - p. 843-853 , 2009
Link: https://doi.org/10.1002/..
 
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11

Deletions of the 3′ BCR and 5′ ABL regions in patients with..:

Fournier, Mickaël ; Lacrosse, Stéphanie ; Jamar, Mauricette..
Cancer Genetics and Cytogenetics.  160 (2005)  2 - p. 184-187 , 2005
Link: https://doi.org/10.1016/..
 
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12

Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three n..:

Rodríguez, Laura ; Guardia, Nieves Martínez ; Herens, Christian...
American Journal of Medical Genetics Part A.  122A (2003)  2 - p. 119-124 , 2003
Link: https://doi.org/10.1002/..
 
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13

Submicroscopic terminal deletions and duplications in retar..:

Riegel, Mariluce ; Baumer, Alessandra ; Jamar, Mauricette...
Human Genetics.  109 (2001)  3 - p. 286-294 , 2001
Link: https://doi.org/10.1007/..
 
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14

Episphalosomic syndrome : a MCA syndrome ressembling Fancon..:

Verloes, Alain ; Jamar, Mauricette ; Dideberg, Vinciane.
Annales de Génétique.  44 (2001)  2 - p. 59-62 , 2001
Link: https://doi.org/10.1016/..
 
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15

GOMBO syndrome: Another ?pseudorecessive? disorder due to a..:

Verloes, Alain ; Lesenfants, Sylviane ; Jamar, Mauricette..
American Journal of Medical Genetics.  95 (2000)  2 - p. 185-186 , 2000
Link: https://doi.org/10.1002/..
 
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