A new case of HDR syndrome with severe female genital tract malformation: comment on "Novel mutation in the gene encoding the GATA3 transcription factor in a Spanish familial case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with female genital tract malformations" by Hernández et al

Am J Med Genet A. 2011 Sep;155A(9):2329-30. doi: 10.1002/ajmg.a.34153. Epub 2011 Aug 10.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Deafness / genetics*
  • Female
  • GATA3 Transcription Factor / genetics*
  • Genitalia, Female / abnormalities*
  • Humans
  • Hypoparathyroidism / genetics*
  • Kidney / abnormalities*

Substances

  • GATA3 Transcription Factor