BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 9602490)

  • 1. High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocation.
    Guichet A; Briault S; Moraine C
    Prenat Diagn; 1998 Apr; 18(4):399-403. PubMed ID: 9602490
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relevance to prenatal diagnosis of the identification of a human Y/autosome translocation by Y-chromosome-specific in situ hybridisation.
    Ellis PM; West JD; West KM; Murray RS; Coyle MC
    Mol Reprod Dev; 1990 Jan; 25(1):37-41. PubMed ID: 2393582
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
    Alves C; Carvalho F; Cremades N; Sousa M; Barros A
    Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization.
    Bernstein R; Bocian ME; Cain MJ; Bengtsson U; Wasmuth JJ
    Am J Med Genet; 1993 Apr; 46(1):77-82. PubMed ID: 8494035
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD; Musci TJ
    Prenat Diagn; 2001 Mar; 21(3):171-5. PubMed ID: 11260602
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
    Balícek P; Jüttnerová V; Jarosová M; Fialová J; Fiedler Z; Kolmanová J
    Cas Lek Cesk; 2001 Mar; 140(4):122-4. PubMed ID: 11284430
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
    Senger G; Chudoba I; Friedrich U; Tommerup N; Claussen U; Brøndum-Nielsen K
    Prenat Diagn; 1997 Apr; 17(4):369-74. PubMed ID: 9160390
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
    Wang H; Li H; Wang H; Wang H; Xia Y; Wen J; Long Z; Dai H; Liang D; Xia J; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exclusion of uniparental inheritance of chromosome 15 in a fetus with a familial dicentric (Y;15) translocation.
    White LM; Treat K; Leff A; Styers D; Mitchell M; Knoll JH
    Prenat Diagn; 1998 Feb; 18(2):111-6. PubMed ID: 9516010
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal detection of a de novo Yqh-acrocentric translocation.
    Ng LK; Kwok YK; Tang LY; Ng PP; Ghosh A; Lau ET; Tang MH
    Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.
    Kleefstra T; van de Zande G; Merkx G; Mieloo H; Hoovers JM; Smeets D
    Eur J Hum Genet; 2000 Aug; 8(8):637-40. PubMed ID: 10951526
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
    Bacino CA; Kashork CD; Davino NA; Shaffer LG
    Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prenatal diagnosis of two pregnancies with risk of chromosomal disorders].
    Cui YX; Huang B; Shi YC; Lu HY; Xia XY; Pan LJ; Huang YF
    Zhonghua Nan Ke Xue; 2007 Jul; 13(7):624-7. PubMed ID: 17725307
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. 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]  

  • 18. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
    Xiao HM; Tan YQ; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells].
    Marguerat P; Gaide AC; Thonney F; Schorderet D
    Rev Med Suisse Romande; 2000 May; 120(5):401-7. PubMed ID: 10911743
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells].
    Huang Y; Sun X; Li Q
    Zhonghua Fu Chan Ke Za Zhi; 1999 Mar; 34(3):153-5. PubMed ID: 11263185
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.