76 related articles for article (PubMed ID: 11263075)
1. [Clinical and genetic consequences of ring chromosome, a structural genome mutation].
Kosztolányi G
Orv Hetil; 2001 Feb; 142(8):379-81. PubMed ID: 11263075
[TBL] [Abstract][Full Text] [Related]
2. Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12.
Davidsson J; Collin A; Oreberg M; Gisselsson D
Clin Genet; 2008 Jan; 73(1):44-9. PubMed ID: 18005181
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The cytogenetic and clinical implications of a ring chromosome 2.
Cote GB; Katsantoni A; Deligeorgis D
Ann Genet; 1981; 24(4):231-5. PubMed ID: 6977305
[TBL] [Abstract][Full Text] [Related]
5. Ring chromosome 15 and 15qs+ mosaic: clinical and cytogenetic behaviour spanning 29 years.
Smith A; den Dulk G; Viersbach R; Michas J
Am J Med Genet; 1991 Sep; 40(4):460-3. PubMed ID: 1746611
[TBL] [Abstract][Full Text] [Related]
6. Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report.
Kosztolányi G; Brecevic L; Bajnòczky K; Schinzel A; Riegel M
Eur J Med Genet; 2011; 54(2):152-6. PubMed ID: 21145991
[TBL] [Abstract][Full Text] [Related]
7. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
[TBL] [Abstract][Full Text] [Related]
8. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
Rossi E; Riegel M; Messa J; Gimelli S; Maraschio P; Ciccone R; Stroppi M; Riva P; Perrotta CS; Mattina T; Memo L; Baumer A; Kucinskas V; Castellan C; Schinzel A; Zuffardi O
J Med Genet; 2008 Mar; 45(3):147-54. PubMed ID: 18006671
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndrome.
Timur AA; Sadgephour A; Graf M; Schwartz S; Libby ED; Driscoll DJ; Wang Q
Ann Hum Genet; 2004 Jul; 68(Pt 4):353-61. PubMed ID: 15225160
[TBL] [Abstract][Full Text] [Related]
11. [The onset of psychiatric disorders and Wilson's disease].
Benhamla T; Tirouche YD; Abaoub-Germain A; Theodore F
Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
[TBL] [Abstract][Full Text] [Related]
12. Ring chromosome 7 in an Indian woman.
Kaur A; Dhillon S; Garg PD; Singh JR
J Intellect Dev Disabil; 2008 Mar; 33(1):87-94. PubMed ID: 18300171
[TBL] [Abstract][Full Text] [Related]
13. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
Bibas Bonet H; Fontenla M; Fauze R; G de Pinat I
Rev Neurol; 2001 Apr 16-30; 32(8):746-50. PubMed ID: 11391511
[TBL] [Abstract][Full Text] [Related]
14. Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.
Laleye A; Alao MJ; Adjagba M; Hans C; Delneste D; Gnamey DK; Ayivi B; Darboux RB
Genet Couns; 2006; 17(1):35-40. PubMed ID: 16719275
[TBL] [Abstract][Full Text] [Related]
15. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
Zollino M; Murdolo M; Marangi G; Pecile V; Galasso C; Mazzanti L; Neri G
Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):257-69. PubMed ID: 18932124
[TBL] [Abstract][Full Text] [Related]
16. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
[TBL] [Abstract][Full Text] [Related]
17. Ring chromosome 13 in an Omani infant boy with mental retardation and multiple congenital anomalies.
Venugopalan P; Kenue RK
Saudi Med J; 2001 Sep; 22(9):800-3. PubMed ID: 11590457
[TBL] [Abstract][Full Text] [Related]
18. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
[TBL] [Abstract][Full Text] [Related]
19. Ring chromosome 4: Wolf syndrome and unspecific developmental anomalies.
Kosztolányi G
Acta Paediatr Hung; 1985; 26(2):157-65. PubMed ID: 4041283
[TBL] [Abstract][Full Text] [Related]
20. [Mechanism of a genetically conditioned failure to thrive shown in a patient with ring chromosome 18].
Heinz-Erian P; Sigmund J; Frisch H; Kazda S; Bindra A; Rhomberg K
Padiatr Padol; 1985; 20(3):231-41. PubMed ID: 4034214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]