These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 12561219)

  • 1. [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]  

  • 2. Chromosomal cryptic insertion of the terminal region and its formative mechanism determined by fluorescence in situ hybridization.
    Tan Y; Lu G
    Chin Med J (Engl); 2002 Jul; 115(7):1039-42. PubMed ID: 12150739
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients.
    Portnoï MF; Aboura A; Tachdjian G; Bouchard P; Dewailly D; Bourcigaux N; Frydman R; Reyss AC; Brisset S; Christin-Maitre S
    Hum Reprod; 2006 Sep; 21(9):2329-34. PubMed ID: 16751643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.
    Cheng DH; Tan YQ; Di YF; Li LY; Lu GX
    Fertil Steril; 2009 Aug; 92(2):828.e3-6. PubMed ID: 19524892
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ectopic nucleolus organizer regions in a patient with premature ovarian failure.
    Lloveras E; Zamora L; Pérez C; Fuster C; Andreu S; Plaja A
    Fertil Steril; 2006 Oct; 86(4):1001.e15-6. PubMed ID: 17027366
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Minute chromosome rearrangement detected by human telomeric band painting probes].
    Qian WP; Tan YM; Tan YQ; Song D; Xu XQ; Li LY; Lu GX
    Yi Chuan; 2006 May; 28(5):518-20. PubMed ID: 16735227
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y
    Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation.
    Lorda-Sanchez IJ; Ibañez AJ; Sanz RJ; Trujillo MJ; Anabitarte ME; Querejeta ME; Rodriguez de Alba M; Gimenez A; Infantes F; Ramos C; Garcia-Sandoval B; Ayuso C
    Ophthalmic Genet; 2000 Sep; 21(3):185-9. PubMed ID: 11035551
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
    Chen CP; Lin CC; Li YC; Hsieh LJ; Lee CC; Wang W
    Fertil Steril; 2006 Nov; 86(5):1514.e1-2. PubMed ID: 17070202
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. Novel X-chromosomal defect associated with abnormal ovarian function.
    Rao L; Babu A; Padmalatha V; Kanakavalli M; Deenadayal M; Singh L
    J Obstet Gynaecol Res; 2005 Feb; 31(1):12-5. PubMed ID: 15669985
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.
    Brezinová J; Zemanová Z; Ransdorfová S; Pavlistová L; Babická L; Housková L; Melichercíková J; Sisková M; Cermák J; Michalová K
    Cancer Genet Cytogenet; 2007 Feb; 173(1):10-6. PubMed ID: 17284364
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A; Demirhan O; Turgut M; Güzel I; Taştemir D
    Genet Couns; 2008; 19(3):301-8. PubMed ID: 18990986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.