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	1.	Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome. [electronic resource] by Schanze, Denny Neubauer, Dorothée Cormier-Daire, Valerie Delrue, Marie-Ange Dieux-Coeslier, Anne Hasegawa, Tomonobu Holmberg, Eva E Koenig, Rainer Krueger, Gabriele Schanze, Ina Seemanova, Eva Shaw, Adam C Vogt, Julie Volleth, Marianne Reis, André Meinecke, Peter Hennekam, Raoul C M Zenker, Martin Producer: 20150511 In: Human mutation vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans. [electronic resource] by Alders, Marielle Hogan, Benjamin M Gjini, Evisa Salehi, Faranak Al-Gazali, Lihadh Hennekam, Eric A Holmberg, Eva E Mannens, Marcel M A M Mulder, Margot F Offerhaus, G Johan A Prescott, Trine E Schroor, Eelco J Verheij, Joke B G M Witte, Merlijn Zwijnenburg, Petra J Vikkula, Mikka Schulte-Merker, Stefan Hennekam, Raoul C Producer: 20100105 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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