Greig cephalopolysyndactyly syndrome : Altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality

• WILLIAMS PG

収録刊行物

• Clin. Genet.

  Clin. Genet. 52 436-441, 1997

詳細情報

• CRID: 1570854175624083968
• NII論文ID: 10021947699
• データソース種別:
  • CiNii Articles