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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]
3. 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 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
5. High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardation. Lam AC, Lam ST, Lai KK, Tong TM, Chau TC. Clin Biochem; 2006 Mar; 39(3):196-202. PubMed ID: 16497288 [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 Jun; 54(4):e425-32. PubMed ID: 21457803 [Abstract] [Full Text] [Related]