BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 8508672)

  • 21. 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]  

  • 22. Prenatal diagnosis of tetrasomy 18p using multiplex fluorescent PCR and comparison with a variety of techniques.
    Irwin DL; Bryan JL; Chan FY; Matthews PL; Healey SC; Peters M; Findlay I
    Genet Test; 2003; 7(1):1-6. PubMed ID: 12820695
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84.
    Blennow E; Nielsen KB
    Clin Genet; 1991 Jun; 39(6):429-33. PubMed ID: 1863990
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Constitutional tetrasomy 18p.
    Bakshi SR; Brahmbhatt MM; Trivedi PJ; Chudoba I
    Indian Pediatr; 2006 Apr; 43(4):357-60. PubMed ID: 16651677
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
    Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
    Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH).
    Li S; Tuck-Muller CM; Martínez JE; Rowley ER; Chen H; Wertelecki W
    Am J Med Genet; 1998 Dec; 80(5):487-90. PubMed ID: 9880213
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Noninvasive prenatal testing aids identification of tetrasomy 18p: A case report.
    Tamaki Y; Katagiri Y; Umemura N; Takeshita N; Morita M
    Case Rep Womens Health; 2020 Jul; 27():e00236. PubMed ID: 32642449
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
    Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Selective chromosome painting using in situ hybridization].
    Pérez Losada A; Woessner S; Solé F; Caballín MR; Florensa L
    Sangre (Barc); 1993 Apr; 38(2):151-4. PubMed ID: 8516730
    [TBL] [Abstract][Full Text] [Related]  

  • 32. M-FISH applications in clinical genetics.
    Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
    Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Isolation and fluorescence in situ hybridization mapping of 60 cosmid clones on human chromosome 18.
    Nakashima H; Sakai M; Inaba R; Imamura T
    Genomics; 1994 Feb; 19(3):577-80. PubMed ID: 8188303
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Prenatal diagnosis of mosaic tetrasomy 18p.
    Chen CP; Ko TM; Su YN; Chern SR; Su JW; Chen YT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Dec; 51(4):625-9. PubMed ID: 23276569
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sequential fluorescence in situ hybridization analysis for trisomy 12 in B-cell chronic lymphocytic leukemia.
    Hjalmar V
    Methods Mol Med; 2005; 115():231-40. PubMed ID: 15998971
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tetrasomy 18p Case Report.
    He Y; Liao JJ; Liu YL; Wen J; Lou JW
    Clin Lab; 2020 Jan; 66(1):. PubMed ID: 32013361
    [TBL] [Abstract][Full Text] [Related]  

  • 38. FISH with Whole Chromosome Painting Probes.
    Kato TA
    Methods Mol Biol; 2023; 2519():99-104. PubMed ID: 36066714
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Detection of abnormal numbers of chromosome 8 with interphase fluorescence in situ hybridization in hematologic malignancies].
    Wang HP; Li GX; Qiao ZH; Wang HW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):395-7. PubMed ID: 15300644
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
    Graf MD; Gill P; Krew M; Schwartz S
    Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.