Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association

Am J Med Genet A. 2012 Jul;158A(7):1785-7. doi: 10.1002/ajmg.a.35391. Epub 2012 May 25.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Anal Canal / abnormalities
  • Cytoskeletal Proteins / genetics*
  • Esophageal Atresia / diagnosis
  • Esophageal Atresia / genetics*
  • Esophagus / abnormalities
  • Gene Dosage*
  • Genetic Association Studies
  • Heart Defects, Congenital / diagnosis
  • Heart Defects, Congenital / genetics*
  • Humans
  • Kidney / abnormalities
  • LIM Domain Proteins / genetics*
  • Limb Deformities, Congenital / diagnosis
  • Limb Deformities, Congenital / genetics*
  • Polymorphism, Single Nucleotide*
  • Spine / abnormalities
  • Trachea / abnormalities
  • Tracheoesophageal Fistula / diagnosis
  • Tracheoesophageal Fistula / genetics*

Substances

  • Cytoskeletal Proteins
  • LIM Domain Proteins
  • LPP protein, human

Supplementary concepts

  • VACTERL association