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
4
Author(s)
Moldovan, O
·
Carvalho, R
·
Medeira, A
Document Type
Letter
Year published
2011
Published
in AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ISSN: 1552-4825
Volume: 155A, Issue: 9, Pages: 2329-2330 (2)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 21834031
Scopus: 2-s2.0-81155161813
Wos: WOS:000294182500051
Source Identifiers
ISSN: 1552-4825
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