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...

Overview

Journal Am J Med Genet A

Specialty Genetics

Date 2011 Aug 12

PMID 21834031

Citations 6

Authors

Oana Moldovan

Raquel Carvalho

Zulmira Jorge

Ana Medeira

Affiliations

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Citing Articles

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