A 117-kb Microdeletion Removing HOXD9–HOXD13 and EVX2 Causes Synpolydactyly

This publication has 35 references indexed in Scilit:

• Initial sequencing and analysis of the human genome
  Nature, 2001
• Interstitial deletion of the long arm of chromosome 2
  Clinical Dysmorphology, 2000
• Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease 1 1Edited by J. Karn
  Journal of Molecular Biology, 1998
• A LINE element is present at the site of a 300-kb deletion starting in intron 10 of the PAX6 gene in a case of familial aniridia
  Human Genetics, 1996
• Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development
  Human Molecular Genetics, 1996
• Altered Growth and Branching Patterns in Synpolydactyly Caused by Mutations in HOXD13
  Science, 1996
• Deletion of chromosome 2q24‐q31 causes characteristic digital anomalies: Case report and review
  American Journal of Medical Genetics, 1995
• Dinculeotide repeat polymorphism in the HOX4E locus
  Human Molecular Genetics, 1993
• Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: Review of brain, cardiac, and limb malformations
  American Journal of Medical Genetics, 1990
• Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46, XX, del(2) (q31q33)
  American Journal of Medical Genetics, 1986