Schoumans J - Search Results

1

Long-term culture of human urothelial cells--a qualitative analysis.

Fossum M, Lundberg F, Holmberg K, Schoumans J, Kratz G, Nordenskjöld A. Fossum M, et al. Among authors: schoumans j. Cells Tissues Organs. 2005;181(1):11-22. doi: 10.1159/000089965. Cells Tissues Organs. 2005. PMID: 16439815

2

22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment.

Lundin J, Söderhäll C, Lundén L, Hammarsjö A, White I, Schoumans J, Läckgren G, Kockum CC, Nordenskjöld A. Lundin J, et al. Among authors: schoumans j. Eur J Med Genet. 2010 Mar-Apr;53(2):61-5. doi: 10.1016/j.ejmg.2009.11.004. Epub 2010 Jan 4. Eur J Med Genet. 2010. PMID: 20045748

3

Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 cases.

Nordgren A, Heyman M, Sahlén S, Schoumans J, Söderhäll S, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: schoumans j. Eur J Haematol. 2002 Jan;68(1):31-41. doi: 10.1034/j.1600-0609.2002.00547.x. Eur J Haematol. 2002. PMID: 11952819

4

Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype.

Nordgren A, Schoumans J, Söderhäll S, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: schoumans j. Br J Haematol. 2001 Sep;114(4):786-93. doi: 10.1046/j.1365-2141.2001.03008.x. Br J Haematol. 2001. PMID: 11564064 Free article.

5

The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial.

Zachariadis V, Gauffin F, Kuchinskaya E, Heyman M, Schoumans J, Blennow E, Gustafsson B, Barbany G, Golovleva I, Ehrencrona H, Cavelier L, Palmqvist L, Lönnerholm G, Nordenskjöld M, Johansson B, Forestier E, Nordgren A; Nordic Society of Pediatric Hematology, Oncology (NOPHO); Swedish Cytogenetic Leukemia Study Group (SCLSG). Zachariadis V, et al. Among authors: schoumans j. Leukemia. 2011 Apr;25(4):622-8. doi: 10.1038/leu.2010.318. Epub 2011 Jan 18. Leukemia. 2011. PMID: 21242996

6

Molecular cytogenetic approach to the diagnosis of splenic lymphoma: a case report of blastoid mantle cell lymphoma.

Björck E, Landgren O, Schoumans J, Christensson B, Björkholm M, MacDonald AP, Nordenskjöld M. Björck E, et al. Among authors: schoumans j. Leuk Lymphoma. 2003 Jul;44(7):1229-34. doi: 10.1080/1042819031000077061. Leuk Lymphoma. 2003. PMID: 12916877 Review.

7

Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding.

Kuchinskaya E, Heyman M, Nordgren A, Schoumans J, Staaf J, Borg A, Söderhäll S, Grandér D, Nordenskjöld M, Blennow E. Kuchinskaya E, et al. Among authors: schoumans j. Br J Haematol. 2008 Mar;140(5):572-7. doi: 10.1111/j.1365-2141.2007.06917.x. Br J Haematol. 2008. PMID: 18275435 Free article.

8

Screening for copy number alterations in loci associated with autism spectrum disorders by two-color multiplex ligation-dependent probe amplification.

Bremer A, Giacobini M, Nordenskjöld M, Brøndum-Nielsen K, Mansouri M, Dahl N, Anderlid B, Schoumans J. Bremer A, et al. Among authors: schoumans j. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):280-5. doi: 10.1002/ajmg.b.30954. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19319887

9

Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.

Nordgren A, Corcoran M, Sääf A, Bremer A, Kluin-Nelemans HC, Schoumans J, Grandér D. Nordgren A, et al. Among authors: schoumans j. Eur J Haematol. 2010 Jan 1;84(1):17-25. doi: 10.1111/j.1600-0609.2009.01334.x. Eur J Haematol. 2010. PMID: 19682064 Review.

10

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

Schoumans J, Ruivenkamp C, Holmberg E, Kyllerman M, Anderlid BM, Nordenskjöld M. Schoumans J, et al. J Med Genet. 2005 Sep;42(9):699-705. doi: 10.1136/jmg.2004.029637. J Med Genet. 2005. PMID: 16141005 Free PMC article.

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