789 related articles for article (PubMed ID: 16259323)
21. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
[TBL] [Abstract][Full Text] [Related]
22. De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.
Dufke A; Singer S; Borell-Kost S; Stotter M; Pflumm DA; Mau-Holzmann UA; Starke H; Mrasek K; Enders H
Cytogenet Genome Res; 2006; 114(3-4):342-50. PubMed ID: 16954677
[TBL] [Abstract][Full Text] [Related]
23. [Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization].
Shen Y; Xue Y; Li J; Pan J; Wu Y; Chen S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):160-3. PubMed ID: 12673589
[TBL] [Abstract][Full Text] [Related]
24. Characterization of a derivative chromosome 17 by fish-technique.
Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
[TBL] [Abstract][Full Text] [Related]
25. Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.
de Pater JM; Govaerts LC; de Man SA; van der Sijs-Bos CJ; Christiaens GC; van Dam WM; Loneus WH; Engelen JJ
Prenat Diagn; 2003 Sep; 23(9):747-51. PubMed ID: 12975787
[TBL] [Abstract][Full Text] [Related]
26. Two unbalanced segregation products due to a maternal t(7;16)inv(16).
Leegte B; Sikkema-Raddatz B; Hordijk R; Davelaar I; van der Veen A; Cobben JM
Prenat Diagn; 2001 Jul; 21(7):550-2. PubMed ID: 11494289
[TBL] [Abstract][Full Text] [Related]
27. [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]
28. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
Zhao L; Li H; Xue YQ; Pan JL; Wu YF; Lu M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):611-4. PubMed ID: 15583994
[TBL] [Abstract][Full Text] [Related]
29. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
[TBL] [Abstract][Full Text] [Related]
31. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
[TBL] [Abstract][Full Text] [Related]
32. [Clinical and laboratory characteristics of two acute lymphoblastic leukemia patients with dicentric (9; 20) (p11 - 13; q11)].
Gong SL; Qiu HY; Li JY; Han FL; Song XM; Huang ZX; Wang JM
Zhonghua Xue Ye Xue Za Zhi; 2006 May; 27(5):306-9. PubMed ID: 16875578
[TBL] [Abstract][Full Text] [Related]
33. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
[TBL] [Abstract][Full Text] [Related]
37. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
38. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
Mechoso B; Vaglio A; Quadrelli A; Mark HF; Huang XL; Milunsky A; Quadrelli R
Fetal Diagn Ther; 2007; 22(4):249-53. PubMed ID: 17369689
[TBL] [Abstract][Full Text] [Related]
39. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.
Cohn AC; Kearns LS; Savarirayan R; Ryan J; Craig JE; Mackey DA
Ophthalmic Genet; 2005 Mar; 26(1):45-53. PubMed ID: 15823925
[TBL] [Abstract][Full Text] [Related]
40. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
