Clinical utility gene card for: Meckel syndrome

Eur J Hum Genet. 2011 Jul;19(7). doi: 10.1038/ejhg.2010.255. Epub 2011 Feb 2.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ciliary Motility Disorders / diagnosis*
  • Ciliary Motility Disorders / genetics*
  • Encephalocele / diagnosis*
  • Encephalocele / genetics*
  • Genetic Testing
  • Humans
  • Polycystic Kidney Diseases / diagnosis*
  • Polycystic Kidney Diseases / genetics*
  • Prenatal Diagnosis
  • Retinitis Pigmentosa

Supplementary concepts

  • Meckel syndrome type 1

Associated data

  • OMIM/#249000
  • OMIM/#603194
  • OMIM/#607361
  • OMIM/#611134
  • OMIM/#611561
  • OMIM/#612284
  • OMIM/609883
  • OMIM/609884
  • OMIM/610142
  • OMIM/610937
  • OMIM/612013
  • OMIM/613277