Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome von Pober, Barbara R, Johnson, Mark, Urban, Zsolt

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Repetitive Thoughts and Repetitive Behaviors in Williams Syndrome von Huston, John C., Thom, Robyn P., Ravichandran, Caitlin T., Mullett, Jennifer E., Moran, Carly, Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.

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Hypercalcemia in Patients with Williams-Beuren Syndrome von Sindhar, Sampat, BS, Lugo, Michael, BS, Levin, Mark D., MD, Danback, Joshua R., BS, Brink, Benjamin D., MS, Yu, Eric, BA, Dietzen, Dennis J., PhD, Clark, Amy L., DO, Purgert, Carolyn A., MD, PhD, Waxler, Jessica L., MS, Elder, Robert W., MD, Pober, Barbara R., MD, Kozel, Beth A., MD, PhD

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Mutations in LRP2 , which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes von Noonan, Kristin M, MacLaughlin, David T, Loscertales, Maria, Robson, Caroline, Walsh, Christopher A, Al-Gazali, Lihadh, Hill, R Sean, Donnai, Dian, Russell, Meaghan K, Bieth, Eric, Devriendt, Koen, Liu, Tianming, Chassaing, Nicolas, Teebi, Ahmad, Pober, Barbara R, Black, Graeme C M, Lacombe, Didier, Donahoe, Patricia K, Kantarci, Sibel

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Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes von Russell, Meaghan K, Longoni, Mauro, Wells, Julie, Maalouf, Faouzi I, Tracy, Adam A, Loscertales, Maria, Ackerman, Kate G, Pober, Barbara R, Lage, Kasper, Bult, Carol J, Donahoe, Patricia K

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Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics von Longoni, Mauro, High, Frances A., Russell, Meaghan K., Kashani, Alireza, Tracy, Adam A., Coletti, Caroline M., Hila, Regis, Shamia, Ahmed, Wells, Julie, Ackerman, Kate G., Wilson, Jay M., Bult, Carol J., Lee, Charles, Lage, Kasper, Pober, Barbara R., Donahoe, Patricia K.

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A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: Clinical features and differential diagnosis von Pober, Barbara R., Longoni, Mauro, Noonan, Kristin M.

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Williams syndrome von Kozel, Beth A., Barak, Boaz, Kim, Chong Ae, Mervis, Carolyn B., Osborne, Lucy R., Porter, Melanie, Pober, Barbara R.

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Diversity of Participants in Williams Syndrome Intervention Studies von Shin, Eva, Ravichandran, Caitlin, Renzi, Danielle, Pober, Barbara R., McDougle, Christopher J., Thom, Robyn P.

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Glucose and lipid metabolism, bone density, and body composition in individuals with Williams syndrome von Shaikh, Sofia, Waxler, Jessica L., Lee, Hang, Grinke, Kathy, Garry, Jamie, Pober, Barbara R., Stanley, Takara L.

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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects von Petit, Florence, Longoni, Mauro, Wells, Julie, Maser, Richard S., Bogenschutz, Eric L., Dysart, Matthew J., Contreras, Hannah T.M., Frénois, Frederic, Pober, Barbara R., Clark, Robin D., Giampietro, Philip F., Ropers, Hilger H., Hu, Hao, Loscertales, Maria, Wagner, Richard, Ai, Xingbin, Brand, Harrison, Jourdain, Anne-Sophie, Delrue, Marie-Ange, Gilbert-Dussardier, Brigitte, Devisme, Louise, Keren, Boris, McCulley, David J., Qiao, Lu, Hernan, Rebecca, Wynn, Julia, Scott, Tiana M., Calame, Daniel G., Coban-Akdemir, Zeynep, Hernandez, Patricia, Hernandez-Garcia, Andres, Yonath, Hagith, Lupski, James R., Shen, Yufeng, Chung, Wendy K., Scott, Daryl A., Bult, Carol J., Donahoe, Patricia K., High, Frances A.

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Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes von Twigg, Stephen R.F., Babbs, Christian, van den Elzen, Marijke E.P., Goriely, Anne, Taylor, Stephen, McGowan, Simon J., Giannoulatou, Eleni, Lonie, Lorne, Ragoussis, Jiannis, Akha, Elham Sadighi, Knight, Samantha J.L., Zechi-Ceide, Roseli M., Hoogeboom, Jeannette A.M., Pober, Barbara R., Toriello, Helga V., Wall, Steven A., Rita Passos-Bueno, M., Brunner, Han G., Mathijssen, Irene M.J., Wilkie, Andrew O.M.

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Buspirone for the Treatment of Generalized Anxiety Disorder in Williams Syndrome: A Case Series von Thom, Robyn P., Keary, Christopher J., Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.

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Williams Syndrome Predisposes to Vascular Stiffness Modified by Antihypertensive Use and Copy Number Changes in NCF1 von Kozel, Beth A, Danback, Joshua R, Waxler, Jessica L, Knutsen, Russell H, de las Fuentes, Lisa, Reusz, Gyorgy S, Kis, Eva, Bhatt, Ami B, Pober, Barbara R

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The proceedings of the 15th professional conference on Williams Syndrome von Walton, Jennifer R., Martens, Marilee A., Pober, Barbara R.

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Frequency of QTc Interval Prolongation in Children and Adults with Williams Syndrome von Brink, Benjamin D., Feinn, Richard, Kozel, Beth A., Billington, Charles J., Liu, Delong, Yu, Eric, Sindhar, Sampat, He, Julie, Rouse, Charles, Lampert, Rachel, Pober, Barbara R., Elder, Robert W.

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Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams–Beuren syndrome von Lugo, Michael, Wong, Zoë C., Billington, Charles J., Parrish, Phoebe C. R., Muldoon, Glennis, Liu, Delong, Pober, Barbara R., Kozel, Beth A.

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Mild macrocytosis in Williams-Beuren syndrome von Yu, Eric, Feinn, Richard, Bona, Robert, Brink, Benjamin, Sindhar, Sampat, Kozel, Beth A., Pober, Barbara R.

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Rapamycin Inhibits Smooth Muscle Cell Proliferation and Obstructive Arteriopathy Attributable to Elastin Deficiency von Li, Wei, Li, Qingle, Qin, Lingfeng, Ali, Rahmat, Qyang, Yibing, Tassabehji, May, Pober, Barbara R, Sessa, William C, Giordano, Frank J, Tellides, George

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Brief Report: Major Depressive Disorder with Psychotic Features in Williams Syndrome: A Case Series von Valdes, Francisca, Keary, Christopher J., Mullett, Jennifer E., Palumbo, Michelle L., Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.

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