Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome

Bibliographic Details
Title:	Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome
Authors:	Dines, Jennifer N., Liu, Yajuan J., Neufeld‐Kaiser, Whitney, Sawyer, Taylor, Ishak, Gisele E., Tully, Hannah M., Racobaldo, Melissa, Sanchez‐Valle, Amarilis, Disteche, Christine M., Juusola, Jane, Torti, Erin, McWalter, Kirsty, Doherty, Dan, Dipple, Katrina M.
Source:	American journal of medical genetics.Part A. 179(9):1783-1790
Availability:	http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100087162241.0x000001&indx=1&recIds=ETOCvdc_100087162241.0x000001
Database:	British Library Document Supply Centre Inside Serials & Conference Proceedings

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ISSN:	15524825
Published in:	American journal of medical genetics.Part A
Language:	English