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                                       Details for article 8 of 28 found articles
 
 
  Molecular Diagnosis and Clinical Characterization of Pseudohypoparathyroidism Type-Ib in a Patient With Mild Albright’s Hereditary Osteodystrophy-Like Features, Epileptic Seizures, and Defective Renal Handling of Uric Acid
 
 
Title: Molecular Diagnosis and Clinical Characterization of Pseudohypoparathyroidism Type-Ib in a Patient With Mild Albright’s Hereditary Osteodystrophy-Like Features, Epileptic Seizures, and Defective Renal Handling of Uric Acid
Author: Unluturk, Ugur
Harmanci, Ayla
Bayraktar, Miyase
Babaoglu, Melih
Yasar, Umit
Varli, Kubilay
Bastepe, Murat
Appeared in: American journal of the medical sciences
Paging: Volume 336 (2008) nr. 1 pages 7 p.
Year: 2008
Contents:
Publisher: Southern Society for Clinical Investigation
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 8 of 28 found articles
 
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