C. Fridman
Department of Biology
Institute of Bioscience
University of São Paulo
Brazil
Name/email consistency: high
- Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene. Fridman, C., Hosomi, N., Varela, M.C., Souza, A.H., Fukai, K., Koiffmann, C.P. Am. J. Med. Genet. A (2003)
- Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients. Fridman, C., Varela, M.C., Kok, F., Diament, A., Koiffmann, C.P. Am. J. Med. Genet. (2000)
- Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome. Fridman, C., Koiffmann, C.P. Am. J. Med. Genet. (2000)
- Prader-Willi syndrome: genetic tests and clinical findings. Fridman, C., Varela, M.C., Kok, F., Setian, N., Koiffmann, C.P. Genet. Test. (2000)