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	1.	Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population. [electronic resource] by Broadbelt, Kevin G Barger, Melissa A Paterson, David S Holm, Ingrid A Haas, Elisabeth A Krous, Henry F Kinney, Hannah C Markianos, Kyriacos Beggs, Alan H Producer: 20100322 In: Pediatric research vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy. [electronic resource] by Böhm, Johann Biancalana, Valérie Dechene, Elizabeth T Bitoun, Marc Pierson, Christopher R Schaefer, Elise Karasoy, Hatice Dempsey, Melissa A Klein, Fabrice Dondaine, Nicolas Kretz, Christine Haumesser, Nicolas Poirson, Claire Toussaint, Anne Greenleaf, Rebecca S Barger, Melissa A Mahoney, Lane J Kang, Peter B Zanoteli, Edmar Vissing, John Witting, Nanna Echaniz-Laguna, Andoni Wallgren-Pettersson, Carina Dowling, James Merlini, Luciano Oldfors, Anders Bomme Ousager, Lilian Melki, Judith Krause, Amanda Jern, Christina Oliveira, Acary S B Petit, Florence Jacquette, Aurélia Chaussenot, Annabelle Mowat, David Leheup, Bruno Cristofano, Michele Poza Aldea, Juan José Michel, Fabrice Furby, Alain Llona, Jose E Barcena Van Coster, Rudy Bertini, Enrico Urtizberea, Jon Andoni Drouin-Garraud, Valérie Béroud, Christophe Prudhon, Bernard Bedford, Melanie Mathews, Katherine Erby, Lori A H Smith, Stephen A Roggenbuck, Jennifer Crowe, Carol A Brennan Spitale, Allison Johal, Sheila C Amato, Anthony A Demmer, Laurie A Jonas, Jessica Darras, Basil T Bird, Thomas D Laurino, Mercy Welt, Selman I Trotter, Cynthia Guicheney, Pascale Das, Soma Mandel, Jean-Louis Beggs, Alan H Laporte, Jocelyn Producer: 20120906 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)