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Genetic counseling for the dystrophinopathies-Practice resource of the National Society of Genetic Counselors.
J Genet Couns. 2024 Apr 29. doi: 10.1002/jgc4.1892. Online ahead of print.
J Genet Couns. 2024.
PMID: 38682751
Review.
Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49-51 deletion phenotype.
Ulm EA, Nagaraj CB, Tian C, Smolarek TA.
Ulm EA, et al.
Mol Genet Genomic Med. 2023 Jan;11(1):e2088. doi: 10.1002/mgg3.2088. Epub 2022 Nov 24.
Mol Genet Genomic Med. 2023.
PMID: 36424846
Free PMC article.
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Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center.
Baker EK, Ulm EA, Belonis A, Brightman DS, Hallinan BE, Leslie ND, Miethke AG, Vawter-Lee M, Wu Y, Pena LDM.
Baker EK, et al. Among authors: ulm ea.
Front Genet. 2022 Jul 22;13:887698. doi: 10.3389/fgene.2022.887698. eCollection 2022.
Front Genet. 2022.
PMID: 35937981
Free PMC article.
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Developmental functions for the Caenorhabditis elegans Sp protein SPTF-3.
Ulm EA, Sleiman SF, Chamberlin HM.
Ulm EA, et al.
Mech Dev. 2011 Sep-Dec;128(7-10):428-41. doi: 10.1016/j.mod.2011.08.003. Epub 2011 Aug 23.
Mech Dev. 2011.
PMID: 21884786
Free article.
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