You are here

  • Home
  • Archive
  • Volume 40, Issue 8
  • Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients

Citation Tools

Article menu
Download PDFPDF
Letters to JMG
Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients

Download to a citation manager

Download the citation for this article by clicking on one of the following citation managers:

Cite this article as:
Álvarez A, del Castillo I, Pera A, et al
Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients
Journal of Medical Genetics 2003;40:636-639.