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Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2019, Volume 1885, pp. 161 - 170
Multiplex Ligation-dependent Probe Amplification (MLPA) is a method to determine the copy number of up to 60 genomic DNA sequences in a single multiplex PCR... 
Gene dosage | Multiplex polymerase chain reaction (PCR) | Multiplex ligation-dependent probe amplification (MLPA) | Trisomy | Amniotic fluid | Aneuploidy | Chorionic villi
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1708, pp. 537 - 549
This chapter describes a method for the rapid assessment of promoter hypermethylation levels or methylation of imprinted regions in human genomic DNA extracted... 
MLPA | FFPE | Methylation-sensitive restriction enzymes paraffin | Genomic DNA | MS-MLPA | Coffalyser.Net | Methylation | DNA - genetics | Paraffin Embedding | DNA Probes | Genomic Imprinting | Promoter Regions, Genetic | DNA Methylation | Multiplex Polymerase Chain Reaction - methods | DNA - analysis | Humans | CpG Islands | Tissue Fixation | DNA - blood
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2017, Volume 1492, pp. 147 - 153
Multiallelic copy number variants are genomic loci that can be present in a range of different copy numbers between individuals. High or low copy numbers of... 
Deletion | Copy number variation | Duplication | MLPA | Capillary electrophoresis | PCR | Genotype | Multiplex Polymerase Chain Reaction - methods | Humans | Alleles | DNA Copy Number Variations
Journal Article
Chemical Communications, ISSN 1359-7345, 11/2013, Volume 49, Issue 85, pp. 10013 - 10015
Journal Article
BMC Cancer, ISSN 1471-2407, 10/2016, Volume 16, Issue 1, p. 811
Journal Article
Clinica Chimica Acta, ISSN 0009-8981, 10/2015, Volume 450, pp. 19 - 24
In Multiplex Ligation-dependent Probe Amplification (MLPA), copy number variants (CNVs) for specific genes are identified after normalization of the amounts of... 
MLPA | CNV detection | DGV | MEDICAL LABORATORY TECHNOLOGY | Time Factors | Humans | Chromosome Aberrations | Polymorphism, Single Nucleotide - genetics | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Multiplex Polymerase Chain Reaction | Intellectual Disability - genetics
Journal Article
Journal Article
INDIAN JOURNAL OF MEDICAL RESEARCH, ISSN 0971-5916, 09/2010, Volume 132, Issue 3, pp. 303 - 311
Background & objectives: Duchenne (DMD) and Becker muscular dystrophy (BM D) are X-linked recessive disorders, caused by mutations in the dystrophin gene.... 
MEDICINE, RESEARCH & EXPERIMENTAL | Becker muscular dystrophy | DIAGNOSIS | CELLS | DUPLICATIONS | PROTEIN | CDNA | IMMUNOLOGY | REARRANGEMENTS | Algorithm | LOCUS | MEDICINE, GENERAL & INTERNAL | Duchenne muscular dystrophy | DNA | multiplex ligation-dependent probe amplification (MLPA) | DELETIONS | PCR
Journal Article