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	1.	Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis. [electronic resource] by Schwenty-Lara, Janina Nürnberger, Annika Borchers, Annette Producer: 20200219 In: Developmental dynamics : an official publication of the American Association of Anatomists vol. 248 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration. [electronic resource] by Schwenty-Lara, Janina Nehl, Denise Borchers, Annette Producer: 20201019 In: Human molecular genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Sema3a plays a role in the pathogenesis of CHARGE syndrome. [electronic resource] by Ufartes, Roser Schwenty-Lara, Janina Freese, Luisa Neuhofer, Christiane Möller, Janika Wehner, Peter van Ravenswaaij-Arts, Conny M A Wong, Monica T Y Schanze, Ina Tzschach, Andreas Bartsch, Oliver Borchers, Annette Pauli, Silke Producer: 20190208 In: Human molecular genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish. [electronic resource] by Young, Teddy Poobalan, Yogavalli Tan, Ee Kim Tao, Shijie Ong, Sheena Wehner, Peter Schwenty-Lara, Janina Lim, Chin Yan Sadasivam, Akila Lovatt, Matthew Wang, Siew Tein Ali, Yusuf Borchers, Annette Sampath, Karuna Dunn, N Ray Producer: 20141028 In: Development (Cambridge, England) vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)