242 related articles for article (PubMed ID: 18160798)
1. Trisomy of medial 15q as result of an analphoid supernumerary ring chromosome detected by CGH and FISH.
Constantinou M; Płowás I; Kałuzewski B
Cytogenet Genome Res; 2007; 119(1-2):165-9. PubMed ID: 18160798
[TBL] [Abstract][Full Text] [Related]
2. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
[TBL] [Abstract][Full Text] [Related]
3. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
5. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature.
Dupont C; Pipiras E; Chantot-Bastaraud S; Verloes A; Baumann C; Wolf JP; Benzacken B
Eur J Hum Genet; 2003 Jun; 11(6):452-6. PubMed ID: 12774038
[TBL] [Abstract][Full Text] [Related]
8. Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
Rowe AG; Abrams L; Qu Y; Chen E; Cotter PD
Am J Med Genet; 2000 Aug; 93(5):393-8. PubMed ID: 10951463
[TBL] [Abstract][Full Text] [Related]
9. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.
McGinniss MJ; Rosenberg C; Stetten G; Schinzel AA; Binkert F; Petersen MB; Kearns WG; Kazazian HH; Pearson PL; Antonarakis SE
Am J Med Genet; 1993 Jul; 46(6):647-51. PubMed ID: 8362906
[TBL] [Abstract][Full Text] [Related]
12. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
13. Supernumerary ring chromosome in a Bednar tumor (pigmented dermatofibrosarcoma protuberans) is composed of interspersed sequences from chromosomes 17 and 22: a fluorescence in situ hybridization and comparative genomic hybridization analysis.
Nishio J; Iwasaki H; Ishiguro M; Ohjimi Y; Yo S; Isayama T; Naito M; Kikuchi M
Genes Chromosomes Cancer; 2001 Mar; 30(3):305-9. PubMed ID: 11170290
[TBL] [Abstract][Full Text] [Related]
14. A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion.
Morava E; Bartsch O; Czako M; Frensel A; Kárteszi J; Kosztolányi GY
Genet Couns; 2003; 14(3):337-42. PubMed ID: 14577679
[TBL] [Abstract][Full Text] [Related]
15. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
[TBL] [Abstract][Full Text] [Related]
16. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
Wanderley HY; Schrander-Stumpel CT; Visser MO; Van Maanen-Op Het Roodt EA; Loneus WH; Engelen JJ
Genet Couns; 2005; 16(3):277-82. PubMed ID: 16259325
[TBL] [Abstract][Full Text] [Related]
17. Pure partial trisomy 7q: two new patients and review.
Rodríguez L; López F; Paisán L; de la Red Mdel M; Ruiz AM; Blanco M; Antelo Cortizas J; Martínez-Frías ML
Am J Med Genet; 2002 Nov; 113(2):218-24. PubMed ID: 12407716
[TBL] [Abstract][Full Text] [Related]
18. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
[TBL] [Abstract][Full Text] [Related]
19. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
