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A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report.
J Med Case Rep. 2016 Jun 13;10(1):156. doi: 10.1186/s13256-016-0921-8.
J Med Case Rep. 2016.
PMID: 27291887
Free PMC article.
Multi-tissue cytogenetic analysis for the diagnosis of mosaic Down syndrome: A case report.
Moncada Arita WA, Perdomo Domínguez ES, Rivera Caballero AY, Espinoza-Moreno NA, Zavala Galeano ME, DuPont BR, Ramos-Zaldívar HM.
Moncada Arita WA, et al.
Clin Case Rep. 2022 Apr 8;10(4):e05604. doi: 10.1002/ccr3.5604. eCollection 2022 Apr.
Clin Case Rep. 2022.
PMID: 35425598
Free PMC article.
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