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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
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Page 1
Molecular and clinical characterization of patients with a ring chromosome 11.
Hansson KB, Gijsbers AC, Oostdijk W, Rehbock JJ, de Snoo F, Ruivenkamp CA, Kant SG. Hansson KB, et al. Eur J Med Genet. 2012 Dec;55(12):708-14. doi: 10.1016/j.ejmg.2012.08.004. Epub 2012 Aug 23. Eur J Med Genet. 2012. PMID: 22975011
Most of the ring chromosomes arise sporadically and parental transmission is rarely observed. We report five patients carrying a ring chromosome 11, with three of the patients belonging to the same family. SNP array analysis was performed to characterize the …
Most of the ring chromosomes arise sporadically and parental transmission is rarely observed. We report five patients carrying a ring …
De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart disease.
Peng Y, Ma R, Zhou Y, Xia Y, Wen J, Zhang Y, Guo R, Li H, Pan Q, Zhang R, Tang C, Liang D, Wu L. Peng Y, et al. Mol Cytogenet. 2015 Nov 9;8:88. doi: 10.1186/s13039-015-0191-y. eCollection 2015. Mol Cytogenet. 2015. PMID: 26557157 Free PMC article.
BACKGROUND: Ring chromosome 11[r (11)] is a rare chromosomal abnormality that forms when both arms of chromosome 11 break, and then reunite with each other. ...These findings provide important information for genetic counseling for this family, and may improv …
BACKGROUND: Ring chromosome 11[r (11)] is a rare chromosomal abnormality that forms when both arms of chromosome 11 bre …
Complex Mosaic Ring Chromosome 11 Associated with Hemizygous Loss of 8.6 Mb of 11q24.2qter in Atypical Jacobsen Syndrome.
Galvão Gomes A, Paiva Grangeiro CH, Silva LR, Oliveira-Gennaro FG, Pereira CS, Joaquim TM, Panepucci RA, Squire JA, Martelli L. Galvão Gomes A, et al. Mol Syndromol. 2017 Jan;8(1):45-49. doi: 10.1159/000452681. Epub 2016 Nov 17. Mol Syndromol. 2017. PMID: 28232783 Free PMC article.
We investigated a boy with features of JBS using classic cytogenetic methods, FISH and high-resolution array CGH. The proband was found to have a mosaic ring chromosome 11 resulting in a hemizygous 11q terminal deletion of 8.6 Mb, leading to a copy number los …
We investigated a boy with features of JBS using classic cytogenetic methods, FISH and high-resolution array CGH. The proband was found to h …
Ring chromosome 11 and cafe-au-lait spots.
Fagan K, Suthers GK, Hardacre G. Fagan K, et al. Am J Med Genet. 1988 Aug;30(4):911-6. doi: 10.1002/ajmg.1320300406. Am J Med Genet. 1988. PMID: 3189413
We report on the segregation of a cytogenetically non-deleted ring chromosome 11 and cafe-au-lait spots in a family. This appears to be the largest inherited ring autosome yet reported....
We report on the segregation of a cytogenetically non-deleted ring chromosome 11 and cafe-au-lait spots in a family. Th …
Complex karyotype including ring chromosome 11 in a patient with acute myeloid leukemia: case report.
Ornellas MHF, Maioli MCP, Lucena SBSG, Bastos EF, Chaves TS, Melo KV, Ribeiro-Carvalho MM, Liehr T, Alves G. Ornellas MHF, et al. Sao Paulo Med J. 2018 Jul-Aug;136(4):361-367. doi: 10.1590/1516-3180.2016.0252150217. Epub 2017 Aug 21. Sao Paulo Med J. 2018. PMID: 28832804 Free PMC article.
CASE REPORT: Here, we describe the case of a 61-year-old obese female with clinically diagnosed AML who presented a complex karyotype involving an uncommon abnormality: ring chromosome 11. Immunophenotypic analysis confirmed the diagnosis. ...
CASE REPORT: Here, we describe the case of a 61-year-old obese female with clinically diagnosed AML who presented a complex karyotype involv …
Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies.
Carella M, Spreafico F, Palumbo O, Storlazzi CT, Tabano S, Miozzo M, Miglionico L, Calvano S, Sindici G, Gamba B, Impera L, Collini P, Zelante L, Radice P, Perotti D. Carella M, et al. Am J Med Genet A. 2010 Jul;152A(7):1756-63. doi: 10.1002/ajmg.a.33420. Am J Med Genet A. 2010. PMID: 20583153
This duplication was found to involve the chromosome of paternal origin, and occurred in tandem on the ring chromosome 11. Despite the constitutive duplication of the paternal 11p15 chromosome region, the patient showed no sign of Beckwith-Wiedemann syndrome. …
This duplication was found to involve the chromosome of paternal origin, and occurred in tandem on the ring chromosome 11 …
31 results