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Sira Korpaisarn
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Sira Korpaisarn
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Sira Korpaisarn
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1
Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features
by
Sira
Korpaisarn
,
Objoon Trachoo
,
Chutintorn Sriphrapradang
Published 2013-01-01
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Article
2
A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease
by
Sira
Korpaisarn
,
Objoon Trachoo
,
Bhakbhoom Panthan
,
Rangsima Aroonroch
,
Ronnarat Suvikapakornkul
,
Chutintorn Sriphrapradang
Published 2017-08-01
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