Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome

J Med Genet. 2004 May;41(5):381-6. doi: 10.1136/jmg.2003.014829.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / metabolism
  • Abnormalities, Multiple / pathology
  • Amino Acid Sequence
  • Embryo, Mammalian / metabolism
  • Female
  • Gene Expression
  • Genetic Diseases, X-Linked / genetics
  • Heart / embryology
  • Humans
  • Hypertelorism / diagnosis
  • Hypertelorism / genetics*
  • Hypertelorism / metabolism
  • Hypospadias / diagnosis
  • Hypospadias / genetics*
  • Hypospadias / metabolism
  • Male
  • Microtubule Proteins / genetics*
  • Molecular Sequence Data
  • Mutation*
  • Myocardium / metabolism
  • Nuclear Proteins / genetics*
  • Pedigree
  • RNA, Messenger / metabolism
  • Rhombencephalon / embryology
  • Rhombencephalon / metabolism
  • Syndrome
  • Transcription Factors / genetics*
  • Ubiquitin-Protein Ligases

Substances

  • Microtubule Proteins
  • Nuclear Proteins
  • RNA, Messenger
  • Transcription Factors
  • MID1 protein, human
  • Ubiquitin-Protein Ligases

Associated data

  • OMIM/145410
  • OMIM/300000