A Gaze Visualizer Tool Implementation Of Gaze Data Into Lighting Rendering Tools Using Radiance And Honeybee For Grasshopper3D von Khanie, Mandana Sarey, Kjaergaard, Susanne V, Johnsen, Mia H. K, Negendahl, Kristoffer, Wienold, Jan, Andersen, Marilyne

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The Danish Fetal Medicine Database: establishment, organization and quality assessment of the first trimester screening program for trisomy 21 in Denmark 2008-2012 von Ekelund, Charlotte K., Petersen, Olav B., Jørgensen, Finn S., Kjaergaard, Susanne, Larsen, Torben, Olesen, Annette W., Skibsted, Lillian, Skovbo, Peter, Sommer, Steffen, Sperling, Lene, Stavnstrup, Benedicte, Størup, Birgitte, Zingenberg, Helle, Uldbjerg, Niels, Miltoft, Caroline B., Noergaard, Lasse, Wulff, Camilla B., Tabor, Ann

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Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies von Kim, Hyung-Goo, Kim, Hyun-Taek, Leach, Natalia T., Lan, Fei, Ullmann, Reinhard, Silahtaroglu, Asli, Kurth, Ingo, Nowka, Anja, Seong, Ihn Sik, Shen, Yiping, Talkowski, Michael E., Ruderfer, Douglas, Lee, Ji-Hyun, Glotzbach, Caron, Ha, Kyungsoo, Kjaergaard, Susanne, Levin, Alex V., Romeike, Bernd F., Kleefstra, Tjitske, Bartsch, Oliver, Elsea, Sarah H., Jabs, Ethylin Wang, MacDonald, Marcy E., Harris, David J., Quade, Bradley J., Ropers, Hans-Hilger, Shaffer, Lisa G., Kutsche, Kerstin, Layman, Lawrence C., Tommerup, Niels, Kalscheuer, Vera M., Shi, Yang, Morton, Cynthia C., Kim, Cheol-Hee, Gusella, James F.

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A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency von Westphal, Vibeke, Kjaergaard, Susanne, Schollen, Els, Martens, Kevin, Grunewald, Stephanie, Schwartz, Marianne, Matthijs, Gert, Freeze, Hudson H

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Genetic and Metabolic Analysis of the First Adult with Congenital Disorder of Glycosylation Type Ib: Long-Term Outcome and Effects of Mannose Supplementation von Westphal, Vibeke, Kjaergaard, Susanne, Davis, Joseph A., Peterson, Sandra M., Skovby, Flemming, Freeze, Hudson H.

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Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations von Hansen, Thomas v. O., Jønson, Lars, Steffensen, Ane Y., Andersen, Mette K., Kjaergaard, Susanne, Gerdes, Anne-Marie, Ejlertsen, Bent, Nielsen, Finn C.

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