Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 42

1.

Immense random colocalization, revealed by automated high content image cytometry, seriously questions FISH as gold standard for detecting EML4-ALK fusion.

Smuk G, Tornóczky T, Pajor L, Chudoba I, Kajtár B, Sárosi V, Pajor G.

Cytometry A. 2018 Jun;93(6):653-661. doi: 10.1002/cyto.a.23489. Epub 2018 May 19.

PMID:
29777599
2.

Two different del(5q) clones in a patient with myelodysplastic syndrome.

Braulke F, Schanz J, Steffens R, Liehr T, Manvelyan M, Chudoba I, Haase D.

Leuk Lymphoma. 2011 Sep;52(9):1811-4. doi: 10.3109/10428194.2011.575968. Epub 2011 Jun 10. No abstract available.

PMID:
21657962
3.

Losses of both products of the Cdkn2a/Arf locus contribute to asbestos-induced mesothelioma development and cooperate to accelerate tumorigenesis.

Altomare DA, Menges CW, Xu J, Pei J, Zhang L, Tadevosyan A, Neumann-Domer E, Liu Z, Carbone M, Chudoba I, Klein-Szanto AJ, Testa JR.

PLoS One. 2011 Apr 19;6(4):e18828. doi: 10.1371/journal.pone.0018828.

4.

The use of M-FISH and M-BAND to define chromosome abnormalities.

Mackinnon RN, Chudoba I.

Methods Mol Biol. 2011;730:203-18. doi: 10.1007/978-1-61779-074-4_15.

PMID:
21431644
5.

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability.

Tyson C, Dawson AJ, Bal S, Tomiuk M, Anderson T, Tucker D, Riordan D, Chudoba I, Morash B, Mhanni A, Chudley AE, McGillivray B, Parslow M, Rappold G, Roeth R, Fawcett C, Qiao Y, Harvard C, Rajcan-Separovic E.

Am J Med Genet A. 2009 Mar;149A(3):490-5. doi: 10.1002/ajmg.a.32535.

PMID:
19213034
6.

Detailed characterization of 7q deletions by multicolor banding (mBAND) in marginal zone cell lymphoma.

Gazzo S, Chudoba I, Traverse-Glehen A, Baseggio L, Felman P, Berger F, Salles G, Hayette S, Magaud JP, Callet-Bauchu E.

Cancer Genet Cytogenet. 2007 Jun;175(2):159-65.

PMID:
17556073
7.

Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome.

Leach NT, Chudoba I, Stewart TV, Holmes LB, Weremowicz S.

Am J Med Genet A. 2007 Jul 1;143A(13):1489-93.

PMID:
17551927
8.

Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle.

Robinson HM, Harrison CJ, Moorman AV, Chudoba I, Strefford JC.

Genes Chromosomes Cancer. 2007 Apr;46(4):318-26.

PMID:
17243167
10.

[Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].

Bocian E, Nowakowska B, Obersztyn E, Borg K, Chudoba I, Kostyk E, Kruczek A, Pietrzyk J, Mazurczak T.

Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):211-25. Polish.

PMID:
17028390
11.

Constitutional tetrasomy 18p.

Bakshi SR, Brahmbhatt MM, Trivedi PJ, Chudoba I.

Indian Pediatr. 2006 Apr;43(4):357-60.

12.

Multicolour banding provides a detailed characterisation of structural abnormalities of chromosome 1 in Burkitt lymphoma.

Zivkovic T, Chudoba I, Bokemeyer C, Dierlamm J.

Br J Haematol. 2006 Jan;132(1):2. No abstract available.

PMID:
16371013
13.

FISH studies on the telomeric regions of the T-cell acute lymphoblastic leukemia cell line CCRF-CEM.

Wick U, Kirsch M, Rauch A, Chudoba I, Lausen B, Efferth T, Gebhart E.

Cytogenet Genome Res. 2005;111(1):34-40.

PMID:
16093718
15.

A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies.

Kline AD, Griffin CA, Haddadin MH, Chudoba I, Morsberger LA, Hawkins AL, Amato RS, Munshi G, Cohen MM.

Am J Med Genet A. 2004 Aug 30;129A(2):124-9.

PMID:
15316975
16.

mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations.

Chudoba I, Hickmann G, Friedrich T, Jauch A, Kozlowski P, Senger G.

Cytogenet Genome Res. 2004;104(1-4):390-3.

PMID:
15162070
17.
18.

A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Seidel J, Heller A, Senger G, Starke H, Chudoba I, Kelbova C, Tönnies H, Neitzel H, Haase C, Beensen V, Zintl F, Claussen U, Liehr T.

Eur J Pediatr. 2003 Sep;162(9):582-8. Epub 2003 Jun 19. Review.

PMID:
12819962
19.

Cytogenetic evolution of human ovarian cell lines associated with chemoresistance and loss of tumorigenicity.

Struski S, Doco-Fenzy M, Koehler M, Chudoba I, Levy F, Masson L, Michel N, Ulrich E, Gruson N, Bénard J, Potron G, Cornillet-Lefebvre P.

Anal Cell Pathol. 2003;25(3):115-22.

20.

Cryptic t(X;18), ins(6;18), and SYT-SSX2 gene fusion in a case of intraneural monophasic synovial sarcoma.

Lestou VS, O'Connell JX, Robichaud M, Salski C, Mathers J, Maguire J, Chudoba I, Sorensen PH, Lam W, Horsman DE.

Cancer Genet Cytogenet. 2002 Oct 15;138(2):153-6.

PMID:
12505262
21.

The DNA-based structure of human chromosome 5 in interphase.

Lemke J, Claussen J, Michel S, Chudoba I, Mühlig P, Westermann M, Sperling K, Rubtsov N, Grummt UW, Ullmann P, Kromeyer-Hauschild K, Liehr T, Claussen U.

Am J Hum Genet. 2002 Nov;71(5):1051-9. Epub 2002 Oct 7.

22.

Multicolor-FICTION: expanding the possibilities of combined morphologic, immunophenotypic, and genetic single cell analyses.

Martín-Subero JI, Chudoba I, Harder L, Gesk S, Grote W, Novo FJ, Calasanz MJ, Siebert R.

Am J Pathol. 2002 Aug;161(2):413-20.

23.

Identification of a dup(5)(p15.3) by multicolor banding.

Riordan D, Vust A, Wickstrom DE, Brown J, Chudley AE, Tomkins D, Chudoba I, Dawson AJ.

Clin Genet. 2002 Apr;61(4):277-82.

PMID:
12030892
24.

Partial trisomy 9p12p21.3 with a normal phenotype.

Stumm M, Müsebeck J, Tönnies H, Volleth M, Lemke J, Chudoba I, Wieacker P.

J Med Genet. 2002 Feb;39(2):141-4. No abstract available.

25.

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.

Tönnies H, Stumm M, Wegner RD, Chudoba I, Kalscheuer V, Neitzel H.

Cytogenet Cell Genet. 2001;93(3-4):188-94.

PMID:
11528111
26.

Improved definition of chromosomal breakpoints using high-resolution multicolour banding.

Lemke J, Chudoba I, Senger G, Stumm M, Loncarevic IF, Henry C, Zabel B, Claussen U.

Hum Genet. 2001 Jun;108(6):478-83.

PMID:
11499672
27.

Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome.

Birnbacher R, Chudoba I, Pirc-Danoewinata H, König M, Kohlhauser C, Schnedl W, Haas OA.

Ann Genet. 2001 Jan-Mar;44(1):13-8. Review.

PMID:
11334612
28.

CBFB/MYH11 fusion in a patient with AML-M4Eo and cytogenetically normal chromosomes 16.

Pirc-Danoewinata H, Dauwerse HG, König M, Chudoba I, Mitterbauer M, Jäger U, Breuning MH, Haas OA.

Genes Chromosomes Cancer. 2000 Oct;29(2):186-91.

PMID:
10959099
29.

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.

Heller A, Seidel J, Hübler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T.

J Med Genet. 2000 Jul;37(7):529-32.

30.
31.

Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.

Heller A, Chudoba I, Bleck C, Senger G, Claussen U, Liehr T.

Int J Oncol. 2000 Mar;16(3):461-8.

PMID:
10675476
32.
33.

Maternal UPD 20 in a hyperactive child with severe growth retardation.

Chudoba I, Franke Y, Senger G, Sauerbrei G, Demuth S, Beensen V, Neumann A, Hansmann I, Claussen U.

Eur J Hum Genet. 1999 Jul;7(5):533-40.

34.

De novo complete trisomy 5p: clinical report and FISH studies.

Reichenbach H, Holland H, Dalitz E, Demandt C, Meiner A, Chudoba I, Lemke J, Claussen U, Froster UG.

Am J Med Genet. 1999 Aug 27;85(5):447-51. Review.

PMID:
10405440
35.

High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes.

Chudoba I, Plesch A, Lörch T, Lemke J, Claussen U, Senger G.

Cytogenet Cell Genet. 1999;84(3-4):156-60.

PMID:
10393418
36.

Overrepresentation of 7q31 and 17q in renal cell carcinomas.

Glukhova L, Goguel AF, Chudoba I, Angevin E, Pavon C, Terrier-Lacombe MJ, Meddeb M, Escudier B, Bernheim A.

Genes Chromosomes Cancer. 1998 Jul;22(3):171-8.

PMID:
9624528
37.

Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.

Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brøndum-Nielsen K.

Prenat Diagn. 1997 Apr;17(4):369-74.

PMID:
9160390
38.

Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas.

Meddeb M, Danglot G, Chudoba I, Vénuat AM, Bénard J, Avet-Loiseau H, Vasseur B, Le Paslier D, Terrier-Lacombe MJ, Hartmann O, Bernheim A.

Genes Chromosomes Cancer. 1996 Nov;17(3):156-65.

PMID:
8946194
39.

Improved detection of chromosome 16 rearrangements in acute myeloid leukemias using 16p and 16q specific microdissection DNA libraries.

Chudoba I, Rubtsov N, Senger G, Junker K, Bleck C, Claussen U.

Oncol Rep. 1996 Sep;3(5):829-32.

PMID:
21594461
40.

Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcoma.

Schwartz HS, Allen GA, Chudoba I, Butler MG.

Cancer Genet Cytogenet. 1992 Jan;58(1):60-5.

41.
42.

[Histopathology of the chorionic villi in the first trimester of pregnancy].

Rüschoff J, Chudoba I, Köhler A.

Gynakologe. 1988 Jun;21(2):104-6. German. No abstract available.

PMID:
3042539

Supplemental Content

Loading ...
Support Center