Prchalova, D., Havlovicova, M., Sterbova, K., Stranecky, V., Hancarova, M., & Sedlacek, Z. (2017). Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: Case report. BMC Med Genet.

Prchalova, Darina, Marketa Havlovicova, Katalin Sterbova, Viktor Stranecky, Miroslava Hancarova, and Zdenek Sedlacek. "Analysis of 31-year-old Patient With SYNGAP1 Gene Defect Points to Importance of Variants in Broader Splice Regions and Reveals Developmental Trajectory of SYNGAP1-associated Phenotype: Case Report." BMC Med Genet 2017.

Prchalova, Darina, et al. "Analysis of 31-year-old Patient With SYNGAP1 Gene Defect Points to Importance of Variants in Broader Splice Regions and Reveals Developmental Trajectory of SYNGAP1-associated Phenotype: Case Report." BMC Med Genet 2017.