A family with a 1.17 Mb deletion of 12q12: refining genotype-phenotype correlation

Am J Med Genet A. 2010 Sep;152A(9):2394-8. doi: 10.1002/ajmg.a.33570.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 12*
  • Family
  • Genotype
  • Humans
  • Infant
  • Male
  • Phenotype