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RASopathies: A significant cause of polyhydramnios?
Mangels R, Blumenfeld YJ, Homeyer M, Mrazek-Pugh B, Hintz SR, Hudgins L. Mangels R, et al. Prenat Diagn. 2021 Feb;41(3):362-367. doi: 10.1002/pd.5862. Epub 2020 Nov 18. Prenat Diagn. 2021. PMID: 33150592
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene.
Zastrow DB, Baudet H, Shen W, Thomas A, Si Y, Weaver MA, Lager AM, Liu J, Mangels R, Dwight SS, Wright MW, Dobrowolski SF, Eilbeck K, Enns GM, Feigenbaum A, Lichter-Konecki U, Lyon E, Pasquali M, Watson M, Blau N, Steiner RD, Craigen WJ, Mao R; ClinGen Inborn Errors of Metabolism Working Group. Zastrow DB, et al. Among authors: mangels r. Hum Mutat. 2018 Nov;39(11):1569-1580. doi: 10.1002/humu.23649. Hum Mutat. 2018. PMID: 30311390 Free PMC article.
Genetic and phenotypic influences on copulatory plug survival in mice.
Mangels R, Young B, Keeble S, Ardekani R, Meslin C, Ferreira Z, Clark NL, Good JM, Dean MD. Mangels R, et al. Heredity (Edinb). 2015 Dec;115(6):496-502. doi: 10.1038/hdy.2015.50. Epub 2015 Jun 24. Heredity (Edinb). 2015. PMID: 26103947 Free PMC article.
11 results