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Prenatal Diagnosis of a Lethal Skeletal Dysplasia.
Harmon D, Feist C, Edwards EA, Sohaey R, Dukhovny S. Harmon D, et al. Among authors: feist c. Neoreviews. 2021 Dec 1;22(12):e859-e865. doi: 10.1542/neo.22-12-e859. Neoreviews. 2021. PMID: 34850149 No abstract available.
Prenatal Diagnosis of Micrognathia.
D'Mello RJ, Kim AJH, Feist C, Sohaey R, Dukhovny S. D'Mello RJ, et al. Among authors: feist c. Neoreviews. 2023 Nov 1;24(11):e753-e762. doi: 10.1542/neo.24-11-e753. Neoreviews. 2023. PMID: 37907406 No abstract available.
A Nonimmune Hydrops Case.
Layoun V, Kim A, Edwards E, Feist C, Dukhovny S. Layoun V, et al. Among authors: feist c. Neoreviews. 2022 Apr 1;23(4):e284-e290. doi: 10.1542/neo.23-4-e284. Neoreviews. 2022. PMID: 35362041 No abstract available.
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations.
Regalado ES, Mellor-Crummey L, De Backer J, Braverman AC, Ades L, Benedict S, Bradley TJ, Brickner ME, Chatfield KC, Child A, Feist C, Holmes KW, Iannucci G, Lorenz B, Mark P, Morisaki T, Morisaki H, Morris SA, Mitchell AL, Ostergaard JR, Richer J, Sallee D, Shalhub S, Tekin M; Montalcino Aortic Consortium; Estrera A, Musolino P, Yetman A, Pyeritz R, Milewicz DM. Regalado ES, et al. Among authors: feist c. Genet Med. 2018 Oct;20(10):1206-1215. doi: 10.1038/gim.2017.245. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300374 Free PMC article.
27 results