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 Hernandez Et Al.
AuthID
P-002-N8Y
P-002-N8Y
