M. Jamar

发表

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

L. Michaux, J. Dogné, I. Luquet, 2012, Annals of Hematology.

Pattern of congenital heart diseases in Rwandan children with genetic defects

A. Hellin, L. Mutesa, J. Caberg, 2014, The Pan African medical journal.

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

A. Verloes, A. Schinzel, A. Baumer, 2001, Human Genetics.

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

V. Bours, L. Mutesa, J. Caberg, 2016, Journal of tropical pediatrics.

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

V. Bours, V. Dideberg, A. Hellin, 2014, BMC Medical Genetics.

Partial trisomy 4q associated with young-onset dopa-responsive parkinsonism.

G. Moonen, V. Bours, G. Garraux, 2012, Archives of neurology.

Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia.

L. Koulischer, M. Jamar, C. Herens, 1999, Clinical and laboratory haematology.

Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis.

L. Koulischer, G. Fillet, N. Schaaf-Lafontaine, 1999, Cancer genetics and cytogenetics.

Inv(12)(q15q24): a nonrandom change associated with myelodysplasia?

L. Koulischer, M. Jamar, C. Herens, 2000, Cancer genetics and cytogenetics.

Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.

A. Verloes, C. Curry, P. Blanchet, 1998, Journal of medical genetics.

Deletions of the 3'BCR and 5'ABL regions in patients with Philadelphia-positive chronic myeloid leukemia: a one-step process occurring in about 10% of the cases without any evidence of genetic instability in the target cells.

V. Bours, M. Jamar, C. Herens, 2005, Cancer genetics and cytogenetics.

Autosomal aneuploidy rate in spermatozoa: a comparison between normospermic and oligospermic males, using a double-color FISH

M. Jamar, C. Hanemann, C. Herens, 2000 .

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

Y. Moreau, F. Speleman, A. Hagemeijer, 2009, Genes, chromosomes & cancer.

Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three new cases and review

A. Verloes, M. Jamar, C. Herens, 2003, American journal of medical genetics. Part A.

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

K. Devriendt, B. Menten, J. Vermeesch, 2020, Prenatal diagnosis.

Cytogenetic study of bovine oocytes matured in vitro.

L. Koulischer, A. Verloes, J. Beckers, 1995, Theriogenology.

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

V. Bours, C. Josse, J. Caberg, 2017, Genes, chromosomes & cancer.

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation.

J. Lupski, J. Wess, P. Chanson, 2014, The New England journal of medicine.

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

Y. Gillerot, L. Koulischer, V. Dideberg, 2001, European Journal of Human Genetics.

Monosomy 11q: report of two familial cases and review of the literature.

R. Hustinx, L. Koulischer, A. Verloes, 1993, American journal of medical genetics.

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

K. Devriendt, B. Menten, J. Vermeesch, 2018, Prenatal diagnosis.

Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13.

V. Bours, A. Hellin, J. Caberg, 2013, Genetic counseling.

Genetic risk in natural and medically assisted procreation.

L. Koulischer, A. Verloes, M. Jamar, 1997, Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy.

A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation

V. Bours, A. Hellin, L. Mutesa, 2012, Indian journal of human genetics.

A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases.

L. Koulischer, V. Bours, M. Jamar, 2003, Genetic counseling.

Episphalosomic syndrome : a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens.

A. Verloes, M. Jamar, C. Herens, 2001, Annales de genetique.

Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome.

L. Koulischer, A. Verloes, J. Lombet, 1997, American journal of medical genetics.

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

Y. Moreau, F. Speleman, A. Hagemeijer, 2009, Genes, chromosomes & cancer.

GOMBO syndrome: another "pseudorecessive" disorder due to a cryptic translocation.

A. Verloes, M. Jamar, C. Herens, 2000, American journal of medical genetics.

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

L. de Leval, G. Fillet, J. Boniver, 2011, British journal of haematology.