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	1.	Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect. [electronic resource] by Ferese, Rosangela Bonetti, Monica Consoli, Federica Guida, Valentina Sarkozy, Anna Lepri, Francesca Romana Versacci, Paolo Gambardella, Stefano Calcagni, Giulio Margiotti, Katia Piceci Sparascio, Francesca Hozhabri, Hossein Mazza, Tommaso Digilio, Maria Cristina Dallapiccola, Bruno Tartaglia, Marco Marino, Bruno Hertog, Jeroen den De Luca, Alessandro Producer: 20190813 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis-van Creveld syndrome. [electronic resource] by Palencia-Campos, Adrian Ullah, Asmat Nevado, Julian Yildirim, Ruken Unal, Edip Ciorraga, Maria Barruz, Pilar Chico, Lucia Piceci-Sparascio, Francesca Guida, Valentina De Luca, Alessandro Kayserili, Hülya Ullah, Irfan Burmeister, Margit Lapunzina, Pablo Ahmad, Wasim Morales, Aixa V Ruiz-Perez, Victor L Producer: 20180524 In: Human molecular genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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