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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: pagnan n. 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.
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update.
Peschel N, Wright JT, Koster MI, Clarke AJ, Tadini G, Fete M, Hadj-Rabia S, Sybert VP, Norderyd J, Maier-Wohlfart S, Fete TJ, Pagnan N, Visinoni AF, Schneider H. Peschel N, et al. Among authors: pagnan n. Genes (Basel). 2022 Dec 10;13(12):2327. doi: 10.3390/genes13122327. Genes (Basel). 2022. PMID: 36553593 Free PMC article.
Ectodermal dysplasias: clinical and molecular review.
Visinoni AF, Lisboa-Costa T, Pagnan NA, Chautard-Freire-Maia EA. Visinoni AF, et al. Among authors: pagnan na. Am J Med Genet A. 2009 Sep;149A(9):1980-2002. doi: 10.1002/ajmg.a.32864. Am J Med Genet A. 2009. PMID: 19681154 Review.
Ectodermal dysplasias: how many?
Freire-Maia N, Lisboa-Costa T, Pagnan NA. Freire-Maia N, et al. Among authors: pagnan na. Am J Med Genet. 2001 Nov 15;104(1):84. doi: 10.1002/ajmg.1586. Am J Med Genet. 2001. PMID: 11746035 No abstract available.
Say syndrome: report of a familial case.
Pagnan NA, Ribeiro EM, Poerner F. Pagnan NA, et al. Am J Med Genet. 1999 Sep 10;86(2):165-7. doi: 10.1002/(sici)1096-8628(19990910)86:2<165::aid-ajmg15>3.0.co;2-1. Am J Med Genet. 1999. PMID: 10449654
Normal outcome after a 45,X/46,XX/46,X,i(Xq) CVS diagnosis.
Gollop TR, Pieri Pde C, Pagnan NA, Naccache NF, Bittencourt EA. Gollop TR, et al. Among authors: pagnan na. Prenat Diagn. 1990 Oct;10(10):689. doi: 10.1002/pd.1970101010. Prenat Diagn. 1990. PMID: 2274495 No abstract available.
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