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	1.	Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register Study. [electronic resource] by Vangkilde, Anders Olsen, Line Hoeffding, Louise K Pedersen, Carsten B Mortensen, Preben B Werge, Thomas Trabjerg, Betina Producer: 20170117 In: Schizophrenia bulletin vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study. [electronic resource] by Hoeffding, Louise K Trabjerg, Betina B Olsen, Line Mazin, Wiktor Sparsø, Thomas Vangkilde, Anders Mortensen, Preben B Pedersen, Carsten B Werge, Thomas Producer: 20170515 In: JAMA psychiatry vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Altered auditory processing and effective connectivity in 22q11.2 deletion syndrome. [electronic resource] by Larsen, Kit Melissa Mørup, Morten Birknow, Michelle Rosgaard Fischer, Elvira Hulme, Oliver Vangkilde, Anders Schmock, Henriette Baaré, William Frans Christiaan Didriksen, Michael Olsen, Line Werge, Thomas Siebner, Hartwig R Garrido, Marta I Producer: 20191112 In: Schizophrenia research vol. 197 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The Danish 22q11 research initiative. [electronic resource] by Schmock, Henriette Vangkilde, Anders Larsen, Kit Melissa Fischer, Elvira Birknow, Michelle Rosgaard Jepsen, Jens Richardt Møllegaard Olesen, Charlotte Skovby, Flemming Plessen, Kerstin Jessica Mørup, Morten Hulme, Ollie Baaré, William Frans Christiaan Didriksen, Michael Siebner, Hartwig Roman Werge, Thomas Olsen, Line Producer: 20160316 In: BMC psychiatry vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. [electronic resource] by Delio, Maria Guo, Tingwei McDonald-McGinn, Donna M Zackai, Elaine Herman, Sean Kaminetzky, Mark Higgins, Anne Marie Coleman, Karlene Chow, Carolyn Jalbrzikowski, Maria Jarlbrzkowski, Maria Bearden, Carrie E Bailey, Alice Vangkilde, Anders Olsen, Line Olesen, Charlotte Skovby, Flemming Werge, Thomas M Templin, Ludivine Busa, Tiffany Philip, Nicole Swillen, Ann Vermeesch, Joris R Devriendt, Koen Schneider, Maude Dahoun, Sophie Eliez, Stephan Schoch, Kelly Hooper, Stephen R Shashi, Vandana Samanich, Joy Marion, Robert van Amelsvoort, Therese Boot, Erik Klaassen, Petra Duijff, Sasja N Vorstman, Jacob Yuen, Tracy Silversides, Candice Chow, Eva Bassett, Anne Frisch, Amos Weizman, Abraham Gothelf, Doron Niarchou, Maria van den Bree, Marianne Owen, Michael J Suñer, Damian Heine Andreo, Jordi Rosell Armando, Marco Vicari, Stefano Digilio, Maria Cristina Auton, Adam Kates, Wendy R Wang, Tao Shprintzen, Robert J Emanuel, Beverly S Morrow, Bernice E Producer: 20130729 In: American journal of human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)