跳转至内容
Merck
CN
  • A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma.

A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma.

Journal of medical genetics (2005-01-07)
T Hienonen, H Sammalkorpi, P Isohanni, R Versteeg, R Karikoski, L A Aaltonen