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Citation: C. Fridman et Cp. Koiffmann, Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes, GENET MOL B, 23(4), 2000, pp. 715-724

Authors: Fridman, C Varela, MC Kok, F Setian, N Koiffmann, CP

Citation: C. Fridman et al., Prader-Willi syndrome: Genetic tests and clinical findings, GENET TEST, 4(4), 2000, pp. 387-392

Authors: Fridman, C Koiffmann, CP

Citation: C. Fridman et Cp. Koiffmann, Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome, AM J MED G, 94(3), 2000, pp. 249-253

Authors: Fridman, C Varela, MC Kok, F Diament, A Koiffmann, CP

Citation: C. Fridman et al., Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients, AM J MED G, 92(5), 2000, pp. 322-327

Authors: Fridman, C Santos, M Ferrari, I Koiffmann, CP

Citation: C. Fridman et al., A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction, CLIN GENET, 57(1), 2000, pp. 86-87

Authors: Schwartzman, JS Zatz, M Vasques, LD Gomes, RR Koiffmann, CP Fridman, C Otto, PG

Citation: Js. Schwartzman et al., Rett syndrome in a boy with a 47,XXY karyotype, AM J HU GEN, 64(6), 1999, pp. 1781-1785