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Modeling AEC-New approaches to study rare genetic disorders.
Koch PJ, Dinella J, Fete M, Siegfried EC, Koster MI. Koch PJ, et al. Among authors: fete m. Am J Med Genet A. 2014 Oct;164A(10):2443-54. doi: 10.1002/ajmg.a.36455. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24665072 Free PMC article. Review.
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.
Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, Tadini G, Pagnan N, Visinoni AF, Bergendal B, Abbott B, Fete T, Stanford C, Butcher C, D'Souza RN, Sybert VP, Morasso MI. Wright JT, et al. Among authors: fete m. Am J Med Genet A. 2019 Mar;179(3):442-447. doi: 10.1002/ajmg.a.61045. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703280 Free PMC article. Review.
Rare diseases of ectoderm: Translating discovery to therapy.
Wright JT, Abbott BM, Salois MN, Gugger JA, Parraga SP, Swanson AK, Fete M, Koster MI. Wright JT, et al. Among authors: fete m. Am J Med Genet A. 2023 Mar;191(3):902-909. doi: 10.1002/ajmg.a.63090. Epub 2022 Dec 19. Am J Med Genet A. 2023. PMID: 36534506
Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging.
Jones KB, Goodwin AF, Landan M, Seidel K, Tran DK, Hogue J, Chavez M, Fete M, Yu W, Hussein T, Johnson R, Huttner K, Jheon AH, Klein OD. Jones KB, et al. Among authors: fete m. Am J Med Genet A. 2013 Jul;161A(7):1585-93. doi: 10.1002/ajmg.a.35959. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23687000 Free PMC article.
Growth failure in focal dermal hypoplasia.
Hsu SC, Bartz S, Pyle L, Fete M, Davis S, Ohman-Hanson R, Fete TJ, Motil KJ. Hsu SC, et al. Among authors: fete m. Am J Med Genet A. 2019 Apr;179(4):628-633. doi: 10.1002/ajmg.a.61051. Epub 2019 Jan 28. Am J Med Genet A. 2019. PMID: 30693654 Free PMC article.
27 results