Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease von Worthey, Elizabeth A, Mayer, Alan N, Syverson, Grant D, Helbling, Daniel, Bonacci, Benedetta B, Decker, Brennan, Serpe, Jaime M, Dasu, Trivikram, Tschannen, Michael R, Veith, Regan L, Basehore, Monica J, Broeckel, Ulrich, Tomita-Mitchell, Aoy, Arca, Marjorie J, Casper, James T, Margolis, David A, Bick, David P, Hessner, Martin J, Routes, John M, Verbsky, James W, Jacob, Howard J, Dimmock, David P

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Hypertrophic Cardiomyopathy: A New Mutation Illustrates the Need for Family-Centered Care von Lee, Daniel D., Veith, Regan L., Dimmock, David P., Samyn, Margaret M.

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Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency von Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Adès, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L

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Views of nonmedical, health system professionals regarding the return of whole genome sequencing incidental findings von Strong, Kimberly A, Zusevics, Kaija L, Bick, David P, Veith, Regan

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In the Absence of Evidentiary Harm, Existing Societal Norms Regarding Parental Authority Should Prevail von Strong, Kimberly A., Derse, Arthur R., Dimmock, David P., Zusevics, Kaija L., Jeruzal, Jessica, Worthey, Elizabeth, Bick, David, Scharer, Gunter, La Pean Kirschner, Alison, Spellecy, Ryan, Farrell, Michael H., Geurts, Jennifer, Veith, Regan, May, Thomas

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Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency von Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Adès, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L

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Altered TGF[beta] signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency von Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Adès, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L

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Altered TGFb signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency von Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Ades, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L

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