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Publications by Núria Camats
Broad Phenotypes in Heterozygous NR5A1 46,XY Patients With a Disorder of Sex Development: An Oligogenic Origin?
European Journal of Human Genetics
Genetics
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46 Xy Disorder; Etiological Classification of the Patient With Sex Development
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46,XY Disorder of Sex Development-Adrenal Insufficiency Due to CYP11A1 Deficiency
A Case Report: 46 XY-disorder of Sexual Development
International Journal of Reproduction, Contraception, Obstetrics and Gynecology
46,XY Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency
Disorder of Sex Development 46,XY Associated With Mutations in the Gene MAP3K1. The Report of Clinical Cases
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46,XX Ovotesticular Disorder of Sex Development
46,XX Testicular Disorder of Sex Development
The Importance of the Multiplex Ligation-Dependent Probe Amplification in the Identification of a Novel Two-Exon Deletion of the NR5A1 Gene in a Patient With 46,XY Differences of Sex Development
Molecular Biology Reports
Medicine
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Molecular Biology
