138 related articles for article (PubMed ID: 8166430)
1. De novo concurrent 5p deletion and distal 17q duplication identified by fluorescence in situ hybridization (FISH).
Szego K; Rauer M; Baratta E; Hoo JJ
Ann Genet; 1993; 36(4):224-7. PubMed ID: 8166430
[TBL] [Abstract][Full Text] [Related]
2. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
Park JP; McDermet MK; Moeschler JB; Wurster-Hill DH
Ann Genet; 1993; 36(4):217-20. PubMed ID: 8166428
[TBL] [Abstract][Full Text] [Related]
3. Molecular and cytogenetic characterization of 9p- abnormalities.
Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
[TBL] [Abstract][Full Text] [Related]
4. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
5. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
Cora T; Acar H; Oran B
Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
[TBL] [Abstract][Full Text] [Related]
6. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
Engelen JJ; Loots WJ; Albrechts JC; Plomp AS; van der Meer SB; Vles JS; Hamers GJ; Geraedts JP
Am J Med Genet; 1998 Feb; 75(4):409-13. PubMed ID: 9482648
[TBL] [Abstract][Full Text] [Related]
7. De novo nonreciprocal translocation 1;8 confirmed by fluorescent in situ hybridization.
Wiley JE; Stout JC; Palmer SM; Kushnick T
Am J Med Genet; 1995 Jul; 57(4):579-80. PubMed ID: 7573132
[TBL] [Abstract][Full Text] [Related]
8. Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization.
Bernstein R; Bocian ME; Cain MJ; Bengtsson U; Wasmuth JJ
Am J Med Genet; 1993 Apr; 46(1):77-82. PubMed ID: 8494035
[TBL] [Abstract][Full Text] [Related]
9. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
10. Promiscuous translocations of chromosome arm 17q in human neuroblastomas.
Lastowska M; Roberts P; Pearson AD; Lewis I; Wolstenholme J; Bown N
Genes Chromosomes Cancer; 1997 Jul; 19(3):143-9. PubMed ID: 9218994
[TBL] [Abstract][Full Text] [Related]
11. Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
Mallo M; Arenillas L; Espinet B; Salido M; Hernández JM; Lumbreras E; del Rey M; Arranz E; Ramiro S; Font P; González O; Renedo M; Cervera J; Such E; Sanz GF; Luño E; Sanzo C; González M; Calasanz MJ; Mayans J; García-Ballesteros C; Amigo V; Collado R; Oliver I; Carbonell F; Bureo E; Insunza A; Yañez L; Muruzabal MJ; Gómez-Beltrán E; Andreu R; León P; Gómez V; Sanz A; Casasola N; Moreno E; Alegre A; Martín ML; Pedro C; Serrano S; Florensa L; Solé F
Haematologica; 2008 Jul; 93(7):1001-8. PubMed ID: 18591625
[TBL] [Abstract][Full Text] [Related]
12. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
[TBL] [Abstract][Full Text] [Related]
13. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
14. Several chromosomes involved in translocations with chromosome 5 shown with fluorescence in situ hybridization in patients with malignant myeloid disorders.
Bram S; Rödjer S; Swolin B
Cancer Genet Cytogenet; 2004 Nov; 155(1):74-8. PubMed ID: 15527906
[TBL] [Abstract][Full Text] [Related]
15. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
17. Characterization of a de novo t(Y;9) (q11.2;q22) by FISH technique.
Conte RA; Kleyman SM; Klein V; Bialer MG; Verma RS
Ann Genet; 1996; 39(1):10-5. PubMed ID: 9297438
[TBL] [Abstract][Full Text] [Related]
18. Duplication 20p identified via fluorescent in situ hybridization.
LeChien KA; McPherson E; Estop AM
Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
[TBL] [Abstract][Full Text] [Related]
19. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
[TBL] [Abstract][Full Text] [Related]
20. Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization.
Zhao J; Gordon PL; Wilroy RS; Martens PR; Tarleton J; Shulman LP; Simpson JL; Elias S; Tharapel AT
Am J Med Genet; 1995 May; 56(4):398-402. PubMed ID: 7604849
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
