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	1.	Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies. [electronic resource] by Millat, Gilles Chanavat, Valérie Rousson, Robert Producer: 20150115 In: Clinica chimica acta; international journal of clinical chemistry vol. 433 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Evaluation of a new high-throughput next-generation sequencing method based on a custom AmpliSeq™ library and ion torrent PGM™ sequencing for the rapid detection of genetic variations in long QT syndrome. [electronic resource] by Millat, Gilles Chanavat, Valérie Rousson, Robert Producer: 20150604 In: Molecular diagnosis & therapy vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac death. [electronic resource] by Chanavat, Valérie Janin, Alexandre Millat, Gilles Producer: 20161017 In: Clinica chimica acta; international journal of clinical chemistry vol. 453 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathy. [electronic resource] by Millat, Gilles Chanavat, Valérie Créhalet, Hervé Rousson, Robert Producer: 20110119 In: Clinica chimica acta; international journal of clinical chemistry vol. 411 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Development of a high resolution melting method for the detection of genetic variations in Long QT Syndrome. [electronic resource] by Millat, Gilles Chanavat, Valérie Créhalet, Hervé Rousson, Robert Producer: 20110310 In: Clinica chimica acta; international journal of clinical chemistry vol. 412 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Rapid, sensitive and inexpensive detection of SCN5A genetic variations by high resolution melting analysis. [electronic resource] by Millat, Gilles Chanavat, Valérie Rodriguez-Lafrasse, Claire Rousson, Robert Producer: 20090601 In: Clinical biochemistry vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Validation of high-resolution DNA melting analysis for mutation scanning of the LMNA gene. [electronic resource] by Millat, Gilles Chanavat, Valérie Julia, Sophie Crehalet, Hervé Bouvagnet, Patrice Rousson, Robert Producer: 20090727 In: Clinical biochemistry vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome. [electronic resource] by Janin, Alexandre Bessière, Francis Georgescu, Tudor Chanavat, Valérie Chevalier, Philippe Millat, Gilles Producer: 20190621 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Next-generation sequencing (NGS) as a fast molecular diagnosis tool for left ventricular noncompaction in an infant with compound mutations in the MYBPC3 gene. [electronic resource] by Schaefer, Elise Helms, Pauline Marcellin, Luc Desprez, Philippe Billaud, Philippe Chanavat, Valérie Rousson, Robert Millat, Gilles Producer: 20141215 In: European journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy. [electronic resource] by Janin, Alexandre Chanavat, Valérie Rollat-Farnier, Pierre-Antoine Bardel, Claire Nguyen, Karine Chevalier, Philippe Eicher, Jean-Christophe Faivre, Laurence Piard, Juliette Albert, Emma Nony, Severine Millat, Gilles Producer: 20210722 In: Human mutation vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)