BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1918 related articles for article (PubMed ID: 16080292)

  • 21. Subtelomeric fish findings in Turkish patients with idiopathic mental retardation.
    Tos T; Vurucu S; Karkucak M; Kozan S; Gul D; Akin R
    Genet Couns; 2013; 24(3):259-64. PubMed ID: 24341139
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
    Koolen DA; Nillesen WM; Versteeg MH; Merkx GF; Knoers NV; Kets M; Vermeer S; van Ravenswaaij CM; de Kovel CG; Brunner HG; Smeets D; de Vries BB; Sistermans EA
    J Med Genet; 2004 Dec; 41(12):892-9. PubMed ID: 15591274
    [TBL] [Abstract][Full Text] [Related]  

  • 23. MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation.
    Palomares M; Delicado A; Lapunzina P; Arjona D; Amiñoso C; Arcas J; Martinez Bermejo A; Fernández L; López Pajares I
    Clin Genet; 2006 Mar; 69(3):228-33. PubMed ID: 16542387
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.
    Rooms L; Reyniers E; Wuyts W; Storm K; van Luijk R; Scheers S; Wauters J; van den Ende J; Biervliet M; Eyskens F; van Goethem G; Laridon A; Ceulemans B; Courtens W; Kooy RF
    Clin Genet; 2006 Jan; 69(1):58-64. PubMed ID: 16451137
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities].
    Borg K; Bocian E; Stankiewicz P; Obersztyn E; Kruczek A; Nowakowska B; Ilnicka A; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):227-46. PubMed ID: 17028391
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Subtelomeric chromosome aberrations: still a lot to learn.
    Moog U; Arens YH; van Lent-Albrechts JC; Huijts PE; Smeets EE; Schrander-Stumpel CT; Engelen JJ
    Clin Genet; 2005 Nov; 68(5):397-407. PubMed ID: 16207207
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.
    Sismani C; Armour JA; Flint J; Girgalli C; Regan R; Patsalis PC
    Eur J Hum Genet; 2001 Jul; 9(7):527-32. PubMed ID: 11464244
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.
    Colleaux L; Rio M; Heuertz S; Moindrault S; Turleau C; Ozilou C; Gosset P; Raoult O; Lyonnet S; Cormier-Daire V; Amiel J; Le Merrer M; Picq M; de Blois MC; Prieur M; Romana S; Cornelis F; Vekemans M; Munnich A
    Eur J Hum Genet; 2001 May; 9(5):319-27. PubMed ID: 11378819
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Six cases of cryptic subtelomeric translocations in four families: the use of subtelomeric FISH probes as a diagnostic tool.
    Paoloni-Giacobino A; Dahoun S; Briault S; Chalumeau A; Till M; Morraine C; Lespinasse J
    Genet Couns; 2006; 17(1):15-28. PubMed ID: 16719273
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
    Kitsiou-Tzeli S; Sismani C; Ioannides M; Bashiardes S; Ketoni A; Touliatou V; Kolialexi A; Mavrou A; Kanavakis E; Patsalis PC
    Eur J Med Genet; 2007; 50(1):73-8. PubMed ID: 17194633
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evaluation of MLPA for the detection of cryptic subtelomeric rearrangements.
    Monfort S; Orellana C; Oltra S; Roselló M; Guitart M; Martínez F
    J Lab Clin Med; 2006 Jun; 147(6):295-300. PubMed ID: 16750667
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients.
    Utine GE; Celik T; Alanay Y; Alikaşifoğlu M; Boduroğlu K; Tunçbilek E; Aktaş D
    Turk J Pediatr; 2009; 51(3):199-206. PubMed ID: 19817261
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Multiplex ligation-dependent probe amplification analysis of subtelomeric chromosome rearrangements in children with idiopathic mental retardation].
    Li MR; Wang XZ; Yang YL; Zhang YH; Xiong H; Bao XH; Zhong N; Wu XR; Pan H
    Zhonghua Yi Xue Za Zhi; 2009 Nov; 89(40):2839-42. PubMed ID: 20137665
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
    Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
    J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA).
    Rooms L; Reyniers E; van Luijk R; Scheers S; Wauters J; Ceulemans B; Van Den Ende J; Van Bever Y; Kooy RF
    Hum Mutat; 2004 Jan; 23(1):17-21. PubMed ID: 14695528
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.
    Saugier-Veber P; Goldenberg A; Drouin-Garraud V; de La Rochebrochard C; Layet V; Drouot N; Le Meur N; Gilbert-Du-Ssardier B; Joly-Hélas G; Moirot H; Rossi A; Tosi M; Frébourg T
    Eur J Hum Genet; 2006 Sep; 14(9):1009-17. PubMed ID: 16773131
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation.
    Rooms L; Reyniers E; van Luijk R; Scheers S; Wauters J; Kooy RF
    Ann Genet; 2004; 47(1):53-9. PubMed ID: 15050874
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 96.