Jamar M - Search Results

1

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

Muys J, Blaumeiser B, Jacquemyn Y, Bandelier C, Brison N, Bulk S, Chiarappa P, Courtens W, De Leener A, De Rademaeker M, Désir J, Destrée A, Devriendt K, Dheedene A, Fieuw A, Fransen E, Gatot JS, Holmgren P, Jamar M, Janssens S, Keymolen K, Lederer D, Menten B, Meuwissen M, Parmentier B, Pichon B, Rombout S, Sznajer Y, Van Den Bogaert A, Van Den Bogaert K, Vanakker O, Vermeesch J, Janssens K. Muys J, et al. Among authors: jamar m. Prenat Diagn. 2018 Dec;38(13):1120-1128. doi: 10.1002/pd.5373. Epub 2018 Nov 14. Prenat Diagn. 2018. PMID: 30334587

2

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

Muys J, Jacquemyn Y, Blaumeiser B, Bourlard L, Brison N, Bulk S, Chiarappa P, De Leener A, De Rademaeker M, Désir J, Destrée A, Devriendt K, Dheedene A, Duquenne A, Fieuw A, Fransen E, Gatot JS, Jamar M, Janssens S, Kerstjens J, Keymolen K, Lederer D, Menten B, Pichon B, Rombout S, Sznajer Y, Van Den Bogaert A, Van Den Bogaert K, Vermeesch J, Janssens K. Muys J, et al. Among authors: jamar m. Prenat Diagn. 2020 Sep;40(10):1272-1283. doi: 10.1002/pd.5751. Epub 2020 Jun 24. Prenat Diagn. 2020. PMID: 32436253

3

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

Jamar M, Lemarchal C, Lemaire V, Koulischer L, Bours V. Jamar M, et al. Genet Couns. 2003;14(4):395-400. Genet Couns. 2003. PMID: 14738112

4

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

Wenric S, Sticca T, Caberg JH, Josse C, Fasquelle C, Herens C, Jamar M, Max S, Gothot A, Caers J, Bours V. Wenric S, et al. Among authors: jamar m. Genet Epidemiol. 2017 Jan;41(1):35-40. doi: 10.1002/gepi.22019. Epub 2016 Nov 10. Genet Epidemiol. 2017. PMID: 27862228 Free article.

5

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

Herens C, Jamar M, Alvarez-Gonzalez ML, Lesenfants S, Lombet J, Bonnivert J, Koulischer L, Verloes A. Herens C, et al. Among authors: jamar m. Am J Med Genet. 1997 Dec 12;73(2):127-31. doi: 10.1002/(sici)1096-8628(19971212)73:2<127::aid-ajmg5>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9409861

6

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

Uwineza A, Caberg JH, Hitayezu J, Hellin AC, Jamar M, Dideberg V, Rusingiza EK, Bours V, Mutesa L. Uwineza A, et al. Among authors: jamar m. BMC Med Genet. 2014 Jul 12;15:79. doi: 10.1186/1471-2350-15-79. BMC Med Genet. 2014. PMID: 25016475 Free PMC article.

7

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

Verloes A, Gillerot Y, Van Maldergem L, Schoos R, Herens C, Jamar M, Dideberg V, Lesenfants S, Koulischer L. Verloes A, et al. Among authors: jamar m. Eur J Hum Genet. 2001 Jan;9(1):1-4. doi: 10.1038/sj.ejhg.5200575. Eur J Hum Genet. 2001. PMID: 11175292

8

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

Uwineza A, Pierquin G, Gaillez S, Jamar M, Hellin AC, Caberg JH, Bours V. Uwineza A, et al. Among authors: jamar m. Genet Couns. 2013;24(2):193-200. Genet Couns. 2013. PMID: 24032290 Free article.

9

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

Sticca T, Caberg JH, Wenric S, Poulet C, Herens C, Jamar M, Josse C, El Guendi S, Max S, Beguin Y, Gothot A, Caers J, Bours V. Sticca T, et al. Among authors: jamar m. Genes Chromosomes Cancer. 2017 Jan;56(1):18-27. doi: 10.1002/gcc.22397. Epub 2016 Aug 18. Genes Chromosomes Cancer. 2017. PMID: 27454822 Free article.

10

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

Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L. Hustinx R, et al. Among authors: jamar m. Am J Med Genet. 1993 Sep 1;47(3):312-7. doi: 10.1002/ajmg.1320470303. Am J Med Genet. 1993. PMID: 8135272 Review.

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