The National Niemann-Pick Type C1 Disease Database: correlation of lipid profiles, mutations, and biochemical phenotypes by Garver, William S., Jelinek, David, Meaney, F. John, Flynn, James, Pettit, Kathleen M., Shepherd, Glen, Heidenreich, Randall A., Vockley, Cate M. Walsh, Castro, Graciela, Francis, Gordon A.

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Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach by Wolfe, Rachel M., Mohsen, Al‐Walid, Walsh Vockley, Cate, Bertrand, Carol A., Nicholls, Robert D., Heiman, Paige, Seibold, Leah M., Vockley, Jerry, Ghaloul‐Gonzalez, Lina

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Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database by Pena, Loren D.M., van Calcar, Sandra C., Hansen, Joyanna, Edick, Mathew J., Walsh Vockley, Cate, Leslie, Nancy, Cameron, Cynthia, Mohsen, Al-Walid, Berry, Susan A., Arnold, Georgianne L., Vockley, Jerry

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The National Niemann-Pick C1 disease database: Report of clinical features and health problems by Garver, William S., Francis, Gordon A., Jelinek, David, Shepherd, Glen, Flynn, James, Castro, Graciela, Walsh Vockley, Cate, Coppock, Donald L., Pettit, Kathleen M., Heidenreich, Randy A., Meaney, F. John

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Identification of 58 novel mutations in Niemann‐Pick disease type C: Correlation with biochemical phenotype and importance of PTC1‐like domains in NPC1 by Park, Walter D., O'Brien, John F., Lundquist, Patrick A., Kraft, Daniel L., Vockley, Cate Walsh, Karnes, Pamela S., Patterson, Marc C., Snow, Karen

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p73 mutations are not detected in sporadic and hereditary breast cancer by SCHWARTZ, D. I, LINDOR, N. M, WALSH-VOCKLEY, C, ROCHE, P. C, MING MAI, SMITH, D. I, WANGUO LIU, COUCH, F. J

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