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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.

AuthorsOana Moldovan, Raquel Carvalho, Zulmira Jorge, Ana Medeira
JournalAmerican journal of medical genetics. Part A (Am J Med Genet A) Vol. 155A Issue 9 Pg. 2329-30 (Sep 2011) ISSN: 1552-4833 [Electronic] United States
PMID21834031 (Publication Type: Letter, Comment)
Chemical References
  • GATA3 Transcription Factor
Topics
  • Deafness (genetics)
  • Female
  • GATA3 Transcription Factor (genetics)
  • Genitalia, Female (abnormalities)
  • Humans
  • Hypoparathyroidism (genetics)
  • Kidney (abnormalities)

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