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.

✍ Scribed by Oana Moldovan; Raquel Carvalho; Zulmira Jorge; Ana Medeira

• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 51 KB
• Volume: 155
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.34153