MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus by Quintero-Rivera, Fabiola, Xi, Qiongchao J, Keppler-Noreuil, Kim M, Lee, Ji Hyun, Higgins, Anne W, Anchan, Raymond M, Roberts, Amy E, Seong, Ihn Sik, Fan, Xueping, Lage, Kasper, Lu, Lily Y, Tao, Joanna, Hu, Xuchen, Berezney, Ronald, Gelb, Bruce D, Kamp, Anna, Moskowitz, Ivan P, Lacro, Ronald V, Lu, Weining, Morton, Cynthia C, Gusella, James F, Maas, Richard L

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Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis by Mukherjee, Kusumika, Ishii, Kana, Pillalamarri, Vamsee, Kammin, Tammy, Atkin, Joan F, Hickey, Scott E, Xi, Qiongchao J, Zepeda, Cinthya J, Gusella, James F, Talkowski, Michael E, Morton, Cynthia C, Maas, Richard L, Liao, Eric C

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Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux by Lu, Weining, van Eerde, Albertien M., Fan, Xueping, Quintero-Rivera, Fabiola, Kulkarni, Shashikant, Ferguson, Heather, Kim, Hyung-Goo, Fan, Yanli, Xi, Qiongchao, Li, Qing-gang, Sanlaville, Damien, Andrews, William, Sundaresan, Vasi, Bi, Weimin, Yan, Jiong, Giltay, Jacques C., Wijmenga, Cisca, de Jong, Tom P. V.M., Feather, Sally A., Woolf, Adrian S., Rao, Yi, Lupski, James R., Eccles, Michael R., Quade, Bradley J., Gusella, James F., Morton, Cynthia C., Maas, Richard L.

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NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects by Lu, Weining, Quintero-Rivera, Fabiola, Fan, Yanli, Alkuraya, Fowzan S, Donovan, Diana J, Xi, Qiongchao, Turbe-Doan, Annick, Li, Qing-Gang, Campbell, Craig G, Shanske, Alan L, Sherr, Elliott H, Ahmad, Ayesha, Peters, Roxana, Rilliet, Benedict, Parvex, Paloma, Bassuk, Alexander G, Harris, David J, Ferguson, Heather, Kelly, Chantal, Walsh, Christopher A, Gronostajski, Richard M, Devriendt, Koenraad, Higgins, Anne, Ligon, Azra H, Quade, Bradley J, Morton, Cynthia C, Gusella, James F, Maas, Richard L

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The cell adhesion gene PVRL3 is associated with congenital ocular defects by Lachke, Salil A., Higgins, Anne W., Inagaki, Maiko, Saadi, Irfan, Xi, Qiongchao, Long, Michelle, Quade, Bradley J., Talkowski, Michael E., Gusella, James F., Fujimoto, Atsuko, Robinson, Michael L., Yang, Ying, Duong, Quynh T., Shapira, Irit, Motro, Benny, Miyoshi, Jun, Takai, Yoshimi, Morton, Cynthia C., Maas, Richard L.

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