171 related articles for article (PubMed ID: 27060323)
1. [Cytogenetic and molecular characterization of a patient with partial 6q trisomy and 1q monosomy].
Qin F; Lu X; Feng Y; Tang P; Niu G; Li F; Zhang J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):231-4. PubMed ID: 27060323
[TBL] [Abstract][Full Text] [Related]
2. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
[TBL] [Abstract][Full Text] [Related]
3. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
4. Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.
Chen CP; Lin SP; Su YN; Chern SR; Su JW; Lee CC; Wang W
Genet Couns; 2012; 23(4):447-55. PubMed ID: 23431743
[TBL] [Abstract][Full Text] [Related]
5. [Improved identification for trisomy 9p and partial trisomy 6q presented in a patient by array-based comparative genomic hybridization].
Zhang J; Cai J; Yang Y; Wang S; Yao F; Huang C; Li H; Li H; Zhang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):829-832. PubMed ID: 27984615
[TBL] [Abstract][Full Text] [Related]
6. Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes.
Kulikowski LD; Bellucco FT; Nogueira SI; Christofolini DM; Smith Mde A; de Mello CB; Brunoni D; Melaragno MI
Am J Med Genet A; 2008 Oct; 146A(20):2663-7. PubMed ID: 18798309
[TBL] [Abstract][Full Text] [Related]
7. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
8. [Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy].
Lin S; Zhang Z; Wu J; Ji Y; Fang Q; Chen B; Zhou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):340-3. PubMed ID: 27264817
[TBL] [Abstract][Full Text] [Related]
9. 1q44-qter trisomy: clinical report and review of the literature.
Lenzini E; Ballarati L; Drigo P; Carrozzi M; Gambel-Benussi D; Giardino D; Petix V; Rizzotto MR; Pecile V
Genet Test Mol Biomarkers; 2009 Feb; 13(1):79-86. PubMed ID: 19309278
[TBL] [Abstract][Full Text] [Related]
10. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients.
Szabó GP; Knegt AC; Ujfalusi A; Balogh E; Szabó T; Oláh É
Am J Med Genet A; 2012 Apr; 158A(4):869-76. PubMed ID: 22407767
[TBL] [Abstract][Full Text] [Related]
11. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
Petković I; Barisić I; Bastić M; Hećimović S; Bago R
Am J Med Genet A; 2003 Jul; 120A(2):266-71. PubMed ID: 12833412
[TBL] [Abstract][Full Text] [Related]
12. Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.
Wu D; Zhang H; Hou Q; Wang H; Wang T; Liao S
Mol Med Rep; 2017 Nov; 16(5):6222-6227. PubMed ID: 28901405
[TBL] [Abstract][Full Text] [Related]
13. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
Delatycki MB; Voullaire L; Francis D; Petrovic V; Robertson A; Webber LM; Slater HR
J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
[TBL] [Abstract][Full Text] [Related]
14. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.
Wieczorek D; Engels H; Viersbach R; Henke B; Schwanitz G; Passarge E
J Med Genet; 1998 Jul; 35(7):545-53. PubMed ID: 9678698
[TBL] [Abstract][Full Text] [Related]
15. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
[TBL] [Abstract][Full Text] [Related]
16. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
Kulikowski LD; Christ LA; Nogueira SI; Brunoni D; Schwartz S; Melaragno MI
Am J Med Genet A; 2006 Jan; 140(1):82-7. PubMed ID: 16333825
[TBL] [Abstract][Full Text] [Related]
17. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
[TBL] [Abstract][Full Text] [Related]
18. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation.
Hosono K; Kawase K; Kurata K; Niimi Y; Saitsu H; Minoshima S; Ohnishi H; Yamamoto T; Hikoya A; Tachibana N; Fukao T; Yamamoto T; Hotta Y
Ophthalmic Genet; 2020 Apr; 41(2):175-182. PubMed ID: 32223580
[No Abstract] [Full Text] [Related]
19. Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques.
Pan Q; Hu H; Han L; Jing X; Liu H; Yang C; Zhang F; Hu Y; Yue H; Ning Y
PLoS One; 2016; 11(5):e0154574. PubMed ID: 27218255
[TBL] [Abstract][Full Text] [Related]
20. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
Zafra de la Rosa G; Venegas-Vega CA; Monroy N; Contreras-Bucio G; Friedrich U; Houman M; Saad A; Fernández P; Kofman-Alfaro S; Cervantes A
Am J Med Genet A; 2005 Jul; 136(3):259-64. PubMed ID: 15957183
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
