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117 related items for PubMed ID: 19953486
1. [Detection of the genetic abnormalities in patients with mental retardation using multiplex ligation-dependent probe amplification assay]. Zhu L, Wang C, Yang X, Wang Y, Liu X, He X. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):644-7. PubMed ID: 19953486 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
12. Pure subtelomeric microduplications as a cause of mental retardation. Ruiter EM, Koolen DA, Kleefstra T, Nillesen WM, Pfundt R, de Leeuw N, Hamel BC, Brunner HG, Sistermans EA, de Vries BB. Clin Genet; 2007 Oct; 72(4):362-8. PubMed ID: 17850634 [Abstract] [Full Text] [Related]
16. Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies. Mihçi E, Ozcan M, Berker-Karaüzüm S, Keser I, Taçoy S, Hapsolat S, Lüleci G. Turk J Pediatr; 2009 Oct; 51(5):453-9. PubMed ID: 20112600 [Abstract] [Full Text] [Related]
17. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries. Jehee FS, Takamori JT, Medeiros PF, Pordeus AC, Latini FR, Bertola DR, Kim CA, Passos-Bueno MR. Eur J Med Genet; 2011 Oct; 54(4):e425-32. PubMed ID: 21457803 [Abstract] [Full Text] [Related]
18. Designing a simple multiplex ligation-dependent probe amplification (MLPA) assay for rapid detection of copy number variants in the genome. Shen Y, Wu BL. J Genet Genomics; 2009 Apr; 36(4):257-65. PubMed ID: 19376486 [Abstract] [Full Text] [Related]