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Multilocus analysis of hypertension: a hierarchical approach.
Williams SM, Ritchie MD, Phillips JA 3rd, Dawson E, Prince M, Dzhura E, Willis A, Semenya A, Summar M, White BC, Addy JH, Kpodonu J, Wong LJ, Felder RA, Jose PA, Moore JH. Williams SM, et al. Among authors: willis a. Hum Hered. 2004;57(1):28-38. doi: 10.1159/000077387. Hum Hered. 2004. PMID: 15133310
Molecular defects in human carbamoy phosphate synthetase I: mutational spectrum, diagnostic and protein structure considerations.
Häberle J, Shchelochkov OA, Wang J, Katsonis P, Hall L, Reiss S, Eeds A, Willis A, Yadav M, Summar S; Urea Cycle Disorders Consortium; Lichtarge O, Rubio V, Wong LJ, Summar M. Häberle J, et al. Among authors: willis a. Hum Mutat. 2011 Jun;32(6):579-89. doi: 10.1002/humu.21406. Epub 2011 May 5. Hum Mutat. 2011. PMID: 21120950 Free PMC article.
Genetic and phenotypic characterization of Parkinson's disease at the clinic-wide level.
Tropea TF, Hartstone W, Amari N, Baum D, Rick J, Suh E, Zhang H, Paul RA, Han N, Zack R, Brody EM, Albuja I, James J, Spindler M, Deik A, Aamodt WW, Dahodwala N, Hamedani A, Lasker A, Hurtig H, Stern M, Weintraub D, Vaswani P, Willis AW, Siderowf A, Xie SX, Van Deerlin V, Chen-Plotkin AS. Tropea TF, et al. Among authors: willis aw. NPJ Parkinsons Dis. 2024 May 3;10(1):97. doi: 10.1038/s41531-024-00690-6. NPJ Parkinsons Dis. 2024. PMID: 38702337 Free PMC article.
1,372 results