RESEARCHDIAGNOSTICSTRANSLATIONOUTREACH
 
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Pignatelli D, Carvalho BL, Palmeiro A, Barros A, Guerreiro SG, Maçut D
The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency. Frontiers in endocrinology 10: 432, 2019.  [Review] 
 doi: 10.3389/fendo.2019.00432 PMID: 31333583.
 
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@ 2014 Ipatimup Institute of Molecular Pathology and Immunology of the University of Porto
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