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162 related items for PubMed ID: 27822861
1. Genotyping Multiallelic Copy Number Variation with Multiplex Ligation-Dependent Probe Amplification (MLPA). de Boer S, White SJ. Methods Mol Biol; 2017; 1492():147-153. PubMed ID: 27822861 [Abstract] [Full Text] [Related]
2. Stuffer-free multiplex ligation-dependent probe amplification based on conformation-sensitive capillary electrophoresis: a novel technology for robust multiplex determination of copy number variation. Shin GW, Jung SH, Yim SH, Chung B, Yeol Jung G, Chung YJ. Electrophoresis; 2012 Oct; 33(19-20):3052-61. PubMed ID: 22965760 [Abstract] [Full Text] [Related]
3. Detection of RB1 Gene Copy Number Variations Using a Multiplex Ligation-Dependent Probe Amplification Method. Dalay N. Methods Mol Biol; 2018 Oct; 1726():7-18. PubMed ID: 29468539 [Abstract] [Full Text] [Related]
4. Multiplex ligation-dependent probe amplification (MLPA) assay for blood group genotyping, copy number quantification, and analysis of RH variants. Veldhuisen B, van der Schoot CE, de Haas M. Immunohematology; 2015 Oct; 31(2):58-61. PubMed ID: 26495890 [Abstract] [Full Text] [Related]
5. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease. Zhang X, Xu Y, Liu D, Geng J, Chen S, Jiang Z, Fu Q, Sun K. BMC Genomics; 2015 May 08; 16(1):364. PubMed ID: 25952753 [Abstract] [Full Text] [Related]
6. Copy number variation and gene rearrangements in CYP2D6 genotyping using multiplex ligation-dependent probe amplification in Koreans. Kim J, Lee SY, Lee KA. Pharmacogenomics; 2012 Jun 08; 13(8):963-73. PubMed ID: 22676200 [Abstract] [Full Text] [Related]
7. Multiplex Ligation-dependent Probe Amplification (MLPA®) for the detection of copy number variation in genomic sequences. Eijk-Van Os PG, Schouten JP. Methods Mol Biol; 2011 Jun 08; 688():97-126. PubMed ID: 20938835 [Abstract] [Full Text] [Related]
8. MLPA-based approach for initial and simultaneous detection of GBA deletions and recombinant alleles in patients affected by Gaucher Disease. Amico G, Grossi S, Vijzelaar R, Lanza F, Mazzotti R, Corsolini F, Ketema M, Filocamo M. Mol Genet Metab; 2016 Dec 08; 119(4):329-337. PubMed ID: 27802905 [Abstract] [Full Text] [Related]
12. An MLPA-based approach for high-resolution genotyping of disease-related multi-allelic CNVs. Marcinkowska-Swojak M, Klonowska K, Figlerowicz M, Kozlowski P. Gene; 2014 Aug 10; 546(2):257-62. PubMed ID: 24942243 [Abstract] [Full Text] [Related]
13. Detection of CCND1 Gene Copy Number Variations Using Multiplex Ligation-Dependent Probe Amplification and Fluorescence In Situ Hybridization Methods. Ooi A, Oyama T. Methods Mol Biol; 2018 Aug 10; 1726():101-109. PubMed ID: 29468547 [Abstract] [Full Text] [Related]
18. Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases. Stuppia L, Antonucci I, Palka G, Gatta V. Int J Mol Sci; 2012 Oct 23; 13(3):3245-3276. PubMed ID: 22489151 [Abstract] [Full Text] [Related]
19. High-Throughput Copy Number Profiling by Digital Multiplex Ligation-Dependent Probe Amplification in Multiple Myeloma. Kosztolányi S, Kiss R, Atanesyan L, Gángó A, de Groot K, Steenkamer M, Jáksó P, Matolcsy A, Kajtár B, Pajor L, Szuhai K, Savola S, Bödör C, Alpár D. J Mol Diagn; 2018 Nov 23; 20(6):777-788. PubMed ID: 30096382 [Abstract] [Full Text] [Related]
20. Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humans. Vendelbosch S, de Boer M, Gouw RA, Ho CK, Geissler J, Swelsen WT, Moorhouse MJ, Lardy NM, Roos D, van den Berg TK, Kuijpers TW. PLoS One; 2013 Nov 23; 8(6):e67619. PubMed ID: 23840750 [Abstract] [Full Text] [Related] Page: [Next] [New Search]