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Results: 1 to 20 of 110

1.

Cryptic terminal chromosome rearrangements in colorectal carcinoma cell lines detected by subtelomeric FISH analysis.

Stewénius Y, Tanke HJ, Wiegant J, Gisselsson D.

Cytogenet Genome Res. 2006;114(3-4):257-62.

PMID:
16954663
[PubMed - indexed for MEDLINE]
2.

Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.

Engels H, Ehrbrecht A, Zahn S, Bosse K, Vrolijk H, White S, Kalscheuer V, Hoovers JM, Schwanitz G, Propping P, Tanke HJ, Wiegant J, Raap AK.

Eur J Hum Genet. 2003 Sep;11(9):643-51.

PMID:
12939649
[PubMed - indexed for MEDLINE]
Free Article
3.

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.

Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G.

Genet Couns. 2005;16(2):129-38.

PMID:
16080292
[PubMed - indexed for MEDLINE]
4.
5.

Molecular cytogenetic characterisation of the colorectal cancer cell line SW480.

Camps J, Mrasek K, Prat E, Weise A, Starke H, Egozcue J, Miró R, Liehr T.

Oncol Rep. 2004 Jun;11(6):1215-8.

PMID:
15138558
[PubMed - indexed for MEDLINE]
6.

Array CGH detection of a cryptic deletion in a complex chromosome rearrangement.

Rosenberg C, Knijnenburg J, Chauffaille Mde L, Brunoni D, Catelani AL, Sloos W, Szuhai K, Tanke HJ.

Hum Genet. 2005 Apr;116(5):390-4. Epub 2005 Feb 22.

PMID:
15726417
[PubMed - indexed for MEDLINE]
7.
8.

Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods.

Erjavec-Skerget A, Stangler-Herodez S, Zagorac A, Zagradisnik B, Kokalj-Vokac N.

Croat Med J. 2006 Dec;47(6):841-50.

PMID:
17167856
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Detecting rearrangements in children using subtelomeric FISH and SKY.

Clarkson B, Pavenski K, Dupuis L, Kennedy S, Meyn S, Nezarati MM, Nie G, Weksberg R, Withers S, Quercia N, Teebi AS, Teshima I.

Am J Med Genet. 2002 Feb 1;107(4):267-74.

PMID:
11840482
[PubMed - indexed for MEDLINE]
10.

Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.

Tosi S, Giudici G, Rambaldi A, Scherer SW, Bray-Ward P, Dirscherl L, Biondi A, Kearney L.

Genes Chromosomes Cancer. 1999 Mar;24(3):213-21.

PMID:
10451701
[PubMed - indexed for MEDLINE]
11.

Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas.

Bayani J, Zielenska M, Pandita A, Al-Romaih K, Karaskova J, Harrison K, Bridge JA, Sorensen P, Thorner P, Squire JA.

Genes Chromosomes Cancer. 2003 Jan;36(1):7-16.

PMID:
12461745
[PubMed - indexed for MEDLINE]
12.

Combined classical and molecular cytogenetic analysis of cancer.

Teixeira MR.

Eur J Cancer. 2002 Aug;38(12):1580-4. Review.

PMID:
12142045
[PubMed - indexed for MEDLINE]
13.

Subtelomeric rearrangements: results from FISH studies in 84 families with idiopathic mental retardation.

Bocian E, Hélias-Rodzewicz Z, Suchenek K, Obersztyn E, Kutkowska-Kaźmierczak A, Stankiewicz P, Kostyk E, Mazurczak T.

Med Sci Monit. 2004 Apr;10(4):CR143-51.

PMID:
15039644
[PubMed - indexed for MEDLINE]
14.

Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines.

Knutsen T, Padilla-Nash HM, Wangsa D, Barenboim-Stapleton L, Camps J, McNeil N, Difilippantonio MJ, Ried T.

Genes Chromosomes Cancer. 2010 Mar;49(3):204-23. doi: 10.1002/gcc.20730.

PMID:
19927377
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.

Karst C, Gross M, Haase D, Wedding U, Höffken K, Liehr T, Mkrtchyan H.

Int J Oncol. 2006 Apr;28(4):891-7.

PMID:
16525638
[PubMed - indexed for MEDLINE]
16.

Paint-assisted microdissection-FISH: Rapid and simple mapping of translocation breakpoints in the embryonal rhabdomyosarcoma cell line RD.

Roberts I, Foster N, Nacheva E, Coleman N.

Cytometry A. 2004 Apr;58(2):177-84.

PMID:
15057971
[PubMed - indexed for MEDLINE]
Free Article
17.

A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay.

Brown J, Jawad M, Twigg SR, Saracoglu K, Sauerbrey A, Thomas AE, Eils R, Harbott J, Kearney L.

Blood. 2002 Apr 1;99(7):2526-31.

PMID:
11895789
[PubMed - indexed for MEDLINE]
Free Article
18.

Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.

Thienpont B, Gewillig M, Fryns JP, Devriendt K, Vermeesch J.

Cytogenet Genome Res. 2006;114(3-4):338-41.

PMID:
16954676
[PubMed - indexed for MEDLINE]
19.

Genome signatures of colon carcinoma cell lines.

Kleivi K, Teixeira MR, Eknaes M, Diep CB, Jakobsen KS, Hamelin R, Lothe RA.

Cancer Genet Cytogenet. 2004 Dec;155(2):119-31.

PMID:
15571797
[PubMed - indexed for MEDLINE]
20.

Cryptic subtelomeric translocations in the 22q13 deletion syndrome.

Praphanphoj V, Goodman BK, Thomas GH, Raymond GV.

J Med Genet. 2000 Jan;37(1):58-61.

PMID:
10633138
[PubMed - indexed for MEDLINE]
Free PMC Article

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