How a Patient Homozygous for a 30-kb Deletion of the C4-CYP 21 Genomic Region Can Have a Nonclassic Form of 21-Hydroxylase Deficiency
Dagmar l’Allemand(Humboldt-Universität zu Berlin), Yves Morel(Centre National de la Recherche Scientifique), Annette Grüters(Unknown), Dirk Schnabel(Humboldt-Universität zu Berlin), Heiko Krude(Humboldt-Universität zu Berlin), Véronique Tardy(Inserm)
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