151 related articles for article (PubMed ID: 10564873)
1. Characterization of a small supernumerary ring marker derived from chromosome 2 by forward and reverse chromosome painting.
Ostroverkhova NV; Nazarenko SA; Rubtsov NB; Nazarenko LP; Bunina EN
Am J Med Genet; 1999 Nov; 87(3):217-20. PubMed ID: 10564873
[TBL] [Abstract][Full Text] [Related]
2. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
3. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
4. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
[TBL] [Abstract][Full Text] [Related]
5. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.
Melnyk AR; Dewald G
Am J Med Genet; 1994 Mar; 50(1):12-4. PubMed ID: 7512788
[TBL] [Abstract][Full Text] [Related]
6. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
[TBL] [Abstract][Full Text] [Related]
7. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ
Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666
[TBL] [Abstract][Full Text] [Related]
8. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
[TBL] [Abstract][Full Text] [Related]
9. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
D'Amato Sizonenko L; Ng D; Oei P; Winship I
Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
[TBL] [Abstract][Full Text] [Related]
10. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
Riegel M; Schinzel A
Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.
Tan-Sindhunata G; Castedo S; Leegte B; Mulder I; vd Veen AY; vd Hout AH; Wiersma TJ; van Essen AJ
Am J Med Genet; 2000 May; 92(2):147-52. PubMed ID: 10797441
[TBL] [Abstract][Full Text] [Related]
13. Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.
Giardino D; Finelli P; Russo S; Gottardi G; Rodeschini O; Atza MG; Natacci F; Larizza L
Am J Med Genet; 2002 Aug; 111(3):319-23. PubMed ID: 12210331
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Interstitial long-arm deletion of chromosome 7 and ectrodactyly.
Tajara EH; Varella-Garcia M; Gusson AC
Am J Med Genet; 1989 Feb; 32(2):192-4. PubMed ID: 2929660
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Generation of FISH probes using laser microbeam microdissection and application to clinical molecular cytogenetics.
Shim SH; Kyhm JH; Chung SR; Kim SR; Park MI; Lee CH; Cho YH
J Microbiol Biotechnol; 2007 Jul; 17(7):1079-82. PubMed ID: 18051316
[TBL] [Abstract][Full Text] [Related]
19. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
20. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
