Munoz, AnaliaRefine your research by the most used items
Author / Editor
- Blouin, Jean-Louis (5)
- Antonarakis, Stylianos (3)
- Fokstuen, Siv (3)
- Failly, Mike (2)
- Lerch, René (2)
- Mach, François (2)
- Perrot, Andreas (2)
- Sigwart, Ulrich (2)
- Avital, Avraham (1)
- Bartoloni Riotto, Lucia (1)
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remove all| Title | Authors / Editors | Date | |
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Multiplex targeted high-throughput sequencing for Mendelian cardiac disorders | Fokstuen, Siv; Makrythanasis, Periklis; Nikolaev, Sergey Igorievich; Santoni, Federico; ... Blouin, Jean-Louis | 2014 |
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Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice | Fokstuen, Siv; Munoz, Analia; Melacini, Paola; Iliceto, Sabino; ... Blouin, Jean-Louis | 2011 |
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DNAI1 mutations explain only 2% of primary ciliary dykinesia | Failly, Mike; Saitta, Alexandra; Munoz, Analia; Falconnet, Emilie; ... Blouin, Jean-Louis | 2008 |
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Candidate gene analysis in three families with acilia syndrome | Wessels, Marja W.; Avital, Avraham; Failly, Mike; Munoz, Analia; ... Willems, Patrick J. | 2008 |
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A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy | Fokstuen, Siv; Lyle, Robert; Munoz, Analia; Gehrig, Corinne; ... Blouin, Jean-Louis | 2008 |
