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Jamar Michelle

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Main Referenced Co-authors
Herens, Christian  (7)
Verloes, Alain  (6)
Koulischer, Lucien  (5)
Bours, Vincent  (2)
Hellin, Anne-Cécile  (2)
Main Referenced Keywords
Female (3); Humans (3); Adolescent (1); Adult (1); Belgium/epidemiology (1);
Main Referenced Disciplines
Genetics & genetic processes (7)
Hematology (1)
Human health sciences: Multidisciplinary, general & others (1)
Biotechnology (1)
Microbiology (1)

Publications (total 9)

The most downloaded
4 downloads
Mutesa, L., Vanbellinghen, J.-F., Hellin, A.-C., Segers, K., Jamar, M., Pierquin, G., & Bours, V. (2009). Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome. Genetic Counseling, 20 (1), 9-17. https://hdl.handle.net/2268/21312

The most cited

37 citations (Scopus®)

Herens, C., Brasseur, E., Jamar, M., Vierset, L., Schoenen, I., & Koulischer, L. (February 1999). Loss of the Y Chromosome in Bone Marrow Cells: Results on 1907 Consecutive Cases of Leukaemia and Preleukaemia. Clinical and Laboratory Haematology, 21 (1), 17-20. doi:10.1046/j.1365-2257.1999.00173.x https://hdl.handle.net/2268/84479

Mutesa, L., Vanbellinghen, J.-F., Hellin, A.-C., Segers, K., Jamar, M., Pierquin, G., & Bours, V. (2009). Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome. Genetic Counseling, 20 (1), 9-17.
Peer Reviewed verified by ORBi

Mutesa, L., Hellin, A.-C., Jamar, M., Pierquin, G., Bours, V., & Verloes, A. (2007). Precocious puberty associated with partial trisomy 18q and monosomy 11q. Genetic Counseling, 18 (2), 201-207.
Peer Reviewed verified by ORBi

Rodriguez, L., Guardia, N. M., Herens, C., Jamar, M., Verloes, A., Lopez, F., Munoz, J. S., & Martinez-Frias, M. L. (01 October 2003). Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three new cases and review [letter to the editor]. American Journal of Medical Genetics. Part A, 122A (2), 119-124. doi:10.1002/ajmg.a.20243
Peer Reviewed verified by ORBi

Verloes, A., Gillerot, Y., Van Maldergem, L., Schoos, R., Herens, C., Jamar, M., Dideberg, V., Lesenfants, S., & Koulischer, L. (January 2001). Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test? European Journal of Human Genetics, 9 (1), 1-4. doi:10.1038/sj.ejhg.5200575
Peer Reviewed verified by ORBi

Scantamburlo, G., Lampertz, S., Jamar, M., Koulischer, L., & Herens, C. (September 2000). Inv(12)(Q15q24): A Nonrandom Change Associated with Myelodysplasia? Cancer Genetics and Cytogenetics, 121 (2), 206-7. doi:10.1016/S0165-4608(99)00172-7
Peer Reviewed verified by ORBi

Herens, C., Brasseur, E., Jamar, M., Vierset, L., Schoenen, I., & Koulischer, L. (February 1999). Loss of the Y Chromosome in Bone Marrow Cells: Results on 1907 Consecutive Cases of Leukaemia and Preleukaemia. Clinical and Laboratory Haematology, 21 (1), 17-20. doi:10.1046/j.1365-2257.1999.00173.x
Peer Reviewed verified by ORBi

Verloes, A., Curry, C., Jamar, M., Herens, C., O'Lague, P., Marks, J., Sarda, P., & Blanchet, P. (November 1998). Juvenile Rheumatoid Arthritis and Del(22q11) Syndrome: A Non-Random Association. Journal of Medical Genetics, 35 (11), 943-7. doi:10.1136/jmg.35.11.943
Peer Reviewed verified by ORBi

Koulischer, L., Verloes, A., Lesenfants, S., Jamar, M., & Herens, C. (September 1997). Genetic Risk in Natural and Medically Assisted Procreation. Early Pregnancy: Biology and Medicine, 3 (3), 164-71.
Peer Reviewed verified by ORBi

Hustinx, R., Verloes, A., Grattagliano, B., Herens, C., Jamar, M., Soyeur, D., Schaaps, J.-P., & Koulischer, L. (01 September 1993). Monosomy 11q: Report of Two Familial Cases and Review of the Literature. American Journal of Medical Genetics, 47 (3), 312-7. doi:10.1002/ajmg.1320470303
Peer Reviewed verified by ORBi

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