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23. Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma. Sawyer JR; Lukacs JL; Thomas EL; Swanson CM; Goosen LS; Sammartino G; Gilliland JC; Munshi NC; Tricot G; Shaughnessy JD; Barlogie B Br J Haematol; 2001 Jan; 112(1):167-74. PubMed ID: 11167798 [TBL] [Abstract][Full Text] [Related]
24. Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9. Bennour A; Sennana H; Laatiri MA; Elloumi M; Khelif A; Saad A Cancer Genet Cytogenet; 2009 Oct; 194(1):30-7. PubMed ID: 19737651 [TBL] [Abstract][Full Text] [Related]
25. Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes. Lengauer C; Eckelt A; Weith A; Endlich N; Ponelies N; Lichter P; Greulich KO; Cremer T Cytogenet Cell Genet; 1991; 56(1):27-30. PubMed ID: 2004552 [TBL] [Abstract][Full Text] [Related]
26. Translocations as a mechanism for homozygous deletion of 13q14 and loss of the ATM gene in a patient with B-cell chronic lymphocytic leukemia. Herholz H; Kern W; Schnittger S; Haferlach T; Dicker F; Haferlach C Cancer Genet Cytogenet; 2007 Apr; 174(1):57-60. PubMed ID: 17350468 [TBL] [Abstract][Full Text] [Related]
27. [Application of chromosome painting to analysis of structural aberration in five cases]. Su G; Qiao H; Shi Z; Su R; Zeng X; Zhao F; Yang H; Huang S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Aug; 15(4):202-5. PubMed ID: 9691125 [TBL] [Abstract][Full Text] [Related]
28. Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: a comparison of locus-specific probe and whole chromosome painting. Anahory T; Hamamah S; Andréo B; Hédon B; Claustres M; Sarda P; Pellestor F Hum Reprod; 2005 Jul; 20(7):1850-4. PubMed ID: 15845597 [TBL] [Abstract][Full Text] [Related]
29. A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure. Lespinasse J; North MO; Paravy C; Brunel MJ; Malzac P; Blouin JL Hum Reprod; 2003 Oct; 18(10):2058-66. PubMed ID: 14507821 [TBL] [Abstract][Full Text] [Related]
30. Chromosome in situ suppression hybridisation in clinical cytogenetics. Hulten MA; Gould CP; Goldman AS; Waters JJ J Med Genet; 1991 Sep; 28(9):577-82. PubMed ID: 1956055 [TBL] [Abstract][Full Text] [Related]
31. Simultaneous detection of centromere-specific probes and chromosome painting libraries by a combination of primed in situ labelling and chromosome painting (PRINS-painting). Hindkjaer J; Brandt CA; Koch J; Lund TB; Kølvraa S; Bolund L Chromosome Res; 1995 Jan; 3(1):41-4. PubMed ID: 7704414 [TBL] [Abstract][Full Text] [Related]
32. Characterization of Robertsonian translocations by using fluorescence in situ hybridization. Wolff DJ; Schwartz S Am J Hum Genet; 1992 Jan; 50(1):174-81. PubMed ID: 1729886 [TBL] [Abstract][Full Text] [Related]
33. Chromosomal rearrangements detected by FISH and G-banding. Hou JW; Wang TR J Formos Med Assoc; 1996 Sep; 95(9):686-91. PubMed ID: 8918057 [TBL] [Abstract][Full Text] [Related]
34. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102 [TBL] [Abstract][Full Text] [Related]
35. Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene. Popovici C; Basset C; Bertucci F; Orsetti B; Adélaide J; Mozziconacci MJ; Conte N; Murati A; Ginestier C; Charafe-Jauffret E; Ethier SP; Lafage-Pochitaloff M; Theillet C; Birnbaum D; Chaffanet M Genes Chromosomes Cancer; 2002 Nov; 35(3):204-18. PubMed ID: 12353263 [TBL] [Abstract][Full Text] [Related]
36. Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes. Pettenati MJ; Von Kap-Herr C; Jackle B; Bobby P; Mowrey P; Schwartz S; Rao PN; Rosnes J Prenat Diagn; 2002 Mar; 22(3):193-7. PubMed ID: 11920892 [TBL] [Abstract][Full Text] [Related]
37. [Study of a familial insertional translocation involving chromosomes 1 and 7 by using fluorescence in situ hybridization]. Tan Y; Li X; Li L; Lu G Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):183-6. PubMed ID: 11402445 [TBL] [Abstract][Full Text] [Related]
38. Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting. Schinzel A; Lorda-Sanchez I; Binkert F; Carter NP; Bebb CE; Ferguson-Smith MA; Eiholzer U; Zachmann M; Robinson WP J Med Genet; 1995 Dec; 32(12):957-61. PubMed ID: 8825924 [TBL] [Abstract][Full Text] [Related]
39. Translocations between two specific human chromosomes detected by three-color "chromosome painting". Lucas JN; Poggensee M; Straume T Cytogenet Cell Genet; 1993; 62(1):11-2. PubMed ID: 8422750 [TBL] [Abstract][Full Text] [Related]
40. Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization. Gribble SM; Roberts I; Grace C; Andrews KM; Green AR; Nacheva EP Cancer Genet Cytogenet; 2000 Apr; 118(1):1-8. PubMed ID: 10731582 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]