Blennow E - Search Results

1

A comparison of different metaphase CGH methods for the detection of cryptic chromosome aberrations of defined size.

Schoumans J, Nielsen K, Jeppesen I, Anderlid BM, Blennow E, Brøndum-Nielsen K, Nordenskjöld M. Schoumans J, et al. Among authors: blennow e. Eur J Hum Genet. 2004 Jun;12(6):447-54. doi: 10.1038/sj.ejhg.5201175. Eur J Hum Genet. 2004. PMID: 15026784

2

Subtelomeric rearrangements detected in patients with idiopathic mental retardation.

Anderlid BM, Schoumans J, Annerén G, Sahlén S, Kyllerman M, Vujic M, Hagberg B, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: blennow e. Am J Med Genet. 2002 Feb 1;107(4):275-84. doi: 10.1002/ajmg.10029. Am J Med Genet. 2002. PMID: 11840483

3

FISH-mapping of a 100-kb terminal 22q13 deletion.

Anderlid BM, Schoumans J, Annerén G, Tapia-Paez I, Dumanski J, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: blennow e. Hum Genet. 2002 May;110(5):439-43. doi: 10.1007/s00439-002-0713-7. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073014

4

Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment.

Anderlid BM, Schoumans J, Hallqvist A, Ståhl Y, Wallin A, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: blennow e. Eur J Hum Genet. 2003 Jan;11(1):89-92. doi: 10.1038/sj.ejhg.5200907. Eur J Hum Genet. 2003. PMID: 12529712

5

Complete characterization of a large marker chromosome by reverse and forward chromosome painting.

Blennow E, Telenius H, Larsson C, de Vos D, Bajalica S, Ponder BA, Nordenskjöld M. Blennow E, et al. Hum Genet. 1992 Dec;90(4):371-4. doi: 10.1007/BF00220461. Hum Genet. 1992. PMID: 1483693

6

Detailed molecular and clinical characterization of three patients with 21q deletions.

Lindstrand A, Malmgren H, Sahlén S, Schoumans J, Nordgren A, Ergander U, Holm E, Anderlid BM, Blennow E. Lindstrand A, et al. Among authors: blennow e. Clin Genet. 2010 Feb;77(2):145-54. doi: 10.1111/j.1399-0004.2009.01289.x. Epub 2009 Oct 23. Clin Genet. 2010. PMID: 19863549

7

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: blennow e. Eur J Haematol. 2002 Jan;68(1):31-41. doi: 10.1034/j.1600-0609.2002.00547.x. Eur J Haematol. 2002. PMID: 11952819

8

[New analytic methods provide answers regarding chromosome aberrations in 1-2 days].

Bui TH, Blennow E, Nordenskjöld M. Bui TH, et al. Among authors: blennow e. Lakartidningen. 2002 Sep 12;99(37):3601-2. Lakartidningen. 2002. PMID: 12362544 Swedish.

9

Prenatal diagnosis: molecular genetics and cytogenetics.

Bui TH, Blennow E, Nordenskjöld M. Bui TH, et al. Among authors: blennow e. Best Pract Res Clin Obstet Gynaecol. 2002 Oct;16(5):629-43. doi: 10.1053/beog.2002.0327. Best Pract Res Clin Obstet Gynaecol. 2002. PMID: 12475544 Review.

10

Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell lines.

Karpova MB, Schoumans J, Blennow E, Ernberg I, Henter JI, Smirnov AF, Nordenskjöld M, Fadeel B. Karpova MB, et al. Among authors: blennow e. Int J Oncol. 2006 Mar;28(3):605-17. Int J Oncol. 2006. PMID: 16465364

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

109 results

Search Page

Filters