The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome

詳細情報 詳細情報について

• CRID

  1361418520936899712

• NII論文ID

  30018400839

• DOI

  10.1093/hmg/7.6.945

• ISSN

  14602083

  http://id.crossref.org/issn/09646906

• データソース種別

  • Crossref
  • CiNii Articles