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American Journal of Medical Genetics|September 20, 2000
Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndromeC Fridman, C P KoiffmannTransplantation Proceedings|November 18, 2009
Potential effect of using ABO-compatible living-donor liver transplantationE Chaib, C Fridman, E MassadJornal De Pediatria|December 4, 2003
[Hypotonic infants and the Prader-Willi Syndrome]C Fridman, F Kok, C P KoiffmannArquivos De Neuro-Psiquiatria|June 1, 1997
[Angelman syndrome: a frequently undiagnosed cause of mental retardation and epilepsy. Case report]C Fridman, F Kok, A Diament, et al.Clinical Genetics|November 27, 1998
Unusual clinical features in an Angelman syndrome patient with uniparental disomy due to a translocation 15q15qC Fridman, M C Varela, R D Nicholls, et al.Science & Justice : Journal of the Forensic Science Society|May 16, 2025
Evaluation of silver mirror chemical delamination on dusted fingermarksR J Accioly, E G Silva, K C Mariotti, et al.Science & Justice : Journal of the Forensic Science Society|September 10, 2025
Fingermark development on silver mirror surfaces: A comparative study between mirror chemical delamination assessment and established techniquesR J Accioly, E G Silva, K C Mariotti, et al.Genetic Testing|February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findingsC Fridman, M C Varela, F Kok, et al.American Journal of Medical Genetics|June 22, 2000
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patientsC Fridman, M C Varela, F Kok, et al.Science & Justice : Journal of the Forensic Science Society|September 10, 2025
Discriminatory power of the Precision ID GlobalFiler™ NGS STR panel v2 in monozygotic twins for forensic applicationsR I B Fonseca, G Valle-Silva, C T Mendes-Junior, et al.Pageof 2