147 related articles for article (PubMed ID: 11295125)
1. [Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization].
Zhu G; Bartsch O; Wan M; Gillessen-Kaesbach G; Passarge E
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):96-9. PubMed ID: 11295125
[TBL] [Abstract][Full Text] [Related]
2. Identification of new translocation breakpoints at 12q13 in lipomas.
Merscher S; Marondel I; Pedeutour F; Gaudray P; Kucherlapati R; Turc-Carel C
Genomics; 1997 Nov; 46(1):70-7. PubMed ID: 9403060
[TBL] [Abstract][Full Text] [Related]
3. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
4. Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection.
Weimer J; Shivakumar S; Danda S; Thomas N; Ralui LP; Jonat W; Arnold N
Fertil Steril; 2007 Dec; 88(6):1677.e9-13. PubMed ID: 17482166
[TBL] [Abstract][Full Text] [Related]
5. [Study of a familial insertional translocation involving chromosomes 1 and 7 by using fluorescence in situ hybridization].
Tan Y; Li X; Li L; Lu G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):183-6. PubMed ID: 11402445
[TBL] [Abstract][Full Text] [Related]
6. [Molecular cytogenetics study in a case with unbalanced chromosome translocation].
Xia J; Yin Z; Dai H; Xue Z; Chen Y; Pan Q; Ning L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Feb; 17(1):10-2. PubMed ID: 10653900
[TBL] [Abstract][Full Text] [Related]
7. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes.
Wirth J; Nothwang HG; van der Maarel S; Menzel C; Borck G; Lopez-Pajares I; Brøndum-Nielsen K; Tommerup N; Bugge M; Ropers HH; Haaf T
J Med Genet; 1999 Apr; 36(4):271-8. PubMed ID: 10227392
[TBL] [Abstract][Full Text] [Related]
8. Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.
Bienvenu T; Der-Sarkissian H; Billuart P; Tissot M; Des Portes V; Brüls T; Chabrolle JP; Chauveau P; Cherry M; Kahn A; Cohen D; Beldjord C; Chelly J; Cherif D
Eur J Hum Genet; 1997; 5(2):105-9. PubMed ID: 9195162
[TBL] [Abstract][Full Text] [Related]
9. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
10. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
11. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
[TBL] [Abstract][Full Text] [Related]
12. Identification of a yeast artificial chromosome spanning the 8q12 translocation breakpoint in pleomorphic adenomas with t(3;8)(p21;q12).
Röijer E; Kas K; Klawitz I; Bullerdiek J; Van de Ven W; Stenman G
Genes Chromosomes Cancer; 1996 Nov; 17(3):166-71. PubMed ID: 8946195
[TBL] [Abstract][Full Text] [Related]
13. [Application of chromosome painting technique to analysis of structural aberration of human chromosomes].
Yang H; Song Y; Liu Q; Li Y; Fu S; Zhang G; Li P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):135-8. PubMed ID: 11295135
[TBL] [Abstract][Full Text] [Related]
14. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
Cantú ES; Khan TA; Pai GS
Am J Med Genet; 1992 Oct; 44(3):340-4. PubMed ID: 1488982
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
Shetty S; Boycott KM; Gillan TL; Bowser K; Parboosingh JS; McInnes B; Chernos JE; Bernier FP
Clin Dysmorphol; 2007 Oct; 16(4):253-6. PubMed ID: 17786117
[TBL] [Abstract][Full Text] [Related]
17. Clinical and experimental study of two cases of myelodysplastic syndrome with t(3; 5) (q25; q34) translocation.
Wu Y; Xue Y; Zhao M; Chen S; Pan J; Lu D
Zhonghua Xue Ye Xue Za Zhi; 2002 Jun; 23(6):304-6. PubMed ID: 12411061
[TBL] [Abstract][Full Text] [Related]
18. Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
Floris C; Rassu S; Boccone L; Gasperini D; Cao A; Crisponi L
Eur J Hum Genet; 2008 Jun; 16(6):696-704. PubMed ID: 18270536
[TBL] [Abstract][Full Text] [Related]
19. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Gribble SM; Prigmore E; Burford DC; Porter KM; Ng BL; Douglas EJ; Fiegler H; Carr P; Kalaitzopoulos D; Clegg S; Sandstrom R; Temple IK; Youings SA; Thomas NS; Dennis NR; Jacobs PA; Crolla JA; Carter NP
J Med Genet; 2005 Jan; 42(1):8-16. PubMed ID: 15635069
[TBL] [Abstract][Full Text] [Related]
20. [Molecular cytogenetic detection of minute chromosomal structural abnormality on the chromosomal terminal regions].
Tan YQ; Li LY; Lu GX
Yi Chuan Xue Bao; 2002 Sep; 29(9):753-6. PubMed ID: 12561219
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
