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.
270 related articles for article (PubMed ID: 16619270)
21. Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays. Bruno DL; Stark Z; Amor DJ; Burgess T; Butler K; Corrie S; Francis D; Ganesamoorthy D; Hills L; James PA; O'Rielly D; Oertel R; Savarirayan R; Prabhakara K; Salce N; Slater HR Hum Mutat; 2011 Dec; 32(12):1500-6. PubMed ID: 21850686 [TBL] [Abstract][Full Text] [Related]
22. Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patients. Tos T; Karaman A; Aksoy A; Tukun A Genet Couns; 2012; 23(2):289-96. PubMed ID: 22876589 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation. Kok K; Dijkhuizen T; Swart YE; Zorgdrager H; van der Vlies P; Fehrmann R; te Meerman GJ; Gerssen-Schoorl KB; van Essen T; Sikkema-Raddatz B; Buys CH Eur J Med Genet; 2005; 48(3):250-62. PubMed ID: 16179221 [TBL] [Abstract][Full Text] [Related]
25. Oligonucleotide microarrays in constitutional genetic diagnosis. Keren B; Le Caignec C Expert Rev Mol Diagn; 2011 Jun; 11(5):521-32. PubMed ID: 21707460 [TBL] [Abstract][Full Text] [Related]
26. [Microarray-based comparative genomic hybridization in the study of constitutional chromosomal abnormalities]. Béri-Dexheimer M; Bonnet C; Chambon P; Brochet K; Grégoire MJ; Jonveaux P Pathol Biol (Paris); 2007 Feb; 55(1):13-8. PubMed ID: 16697120 [TBL] [Abstract][Full Text] [Related]
27. Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors. Dougherty MJ; Tooke LS; Sullivan LM; Hakonarson H; Wainwright LM; Biegel JA Cancer Genet; 2012; 205(1-2):42-54. PubMed ID: 22429597 [TBL] [Abstract][Full Text] [Related]
34. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods]. Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989 [TBL] [Abstract][Full Text] [Related]
35. Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities. Gouas L; Goumy C; Véronèse L; Tchirkov A; Vago P Pathol Biol (Paris); 2008 Sep; 56(6):345-53. PubMed ID: 18513889 [TBL] [Abstract][Full Text] [Related]
36. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion. Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151 [TBL] [Abstract][Full Text] [Related]
37. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization. del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307 [TBL] [Abstract][Full Text] [Related]
38. Prospective screening of patients with unexplained mental retardation using subtelomeric MLPA strongly increases the detection rate of cryptic unbalanced chromosomal rearrangements. Stegmann AP; Jonker LM; Engelen JJ Eur J Med Genet; 2008; 51(2):93-105. PubMed ID: 18032123 [TBL] [Abstract][Full Text] [Related]