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Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.
Clin Case Rep. 2022 Feb 7;10(2):e05370. doi: 10.1002/ccr3.5370. eCollection 2022 Feb.
Clin Case Rep. 2022.
PMID: 35154720
Free PMC article.
A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature review.
Hu X, Ayala SS, Dyer L, Guan Q, Pena L.
Hu X, et al. Among authors: ayala ss.
Am J Med Genet A. 2021 Jun;185(6):1864-1869. doi: 10.1002/ajmg.a.62166. Epub 2021 Mar 24.
Am J Med Genet A. 2021.
PMID: 33759348
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Efficacy and Safety of Epratuzumab in Moderately to Severely Active Systemic Lupus Erythematosus: Results From Two Phase III Randomized, Double-Blind, Placebo-Controlled Trials.
Clowse ME, Wallace DJ, Furie RA, Petri MA, Pike MC, Leszczyński P, Neuwelt CM, Hobbs K, Keiserman M, Duca L, Kalunian KC, Galateanu C, Bongardt S, Stach C, Beaudot C, Kilgallen B, Gordon C; EMBODY Investigator Group.
Clowse ME, et al.
Arthritis Rheumatol. 2017 Feb;69(2):362-375. doi: 10.1002/art.39856.
Arthritis Rheumatol. 2017.
PMID: 27598855
Free PMC article.
Clinical Trial.
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