Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?
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| Title: | Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed? |
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| Authors: | Manero-Azua A; Rare Diseases Research Group, Molecular (Epi) Genetics Laboratory, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, Araba, Spain., Pereda A; Rare Diseases Research Group, Molecular (Epi) Genetics Laboratory, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, Araba, Spain., Llano-Rivas I; Service of Genetics, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain., Garin I; Service of Genetics, Hospital Universitario Cruces, Barakaldo, Bizkaia, Spain., Perez de Nanclares G; Rare Diseases Research Group, Molecular (Epi) Genetics Laboratory, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, Araba, Spain. |
| Source: | Frontiers in genetics [Front Genet] 2023 Oct 03; Vol. 14, pp. 1274056. Date of Electronic Publication: 2023 Oct 03 (Print Publication: 2023). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2023.1274056 |
