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  1. Article

    RELATIONSHIP BETWEEN GENOTYPE AND PHENOTYPE TN GERMAN FAMILIES WITH CONGENITAL ADRENAL HYPERPLASIA (CAH) DUE TO 21 HYDROXYLASE DEFICIENCY

    In 13 unrelated CAH families (2 with 2 patients) from Berlin, Germany, the CYP21B gene and its region were studied to establish if the incidence of each genetic lesion and the relationship between genotype and...

    A Serban, D L'Allemand, H Helge, M Murena, Y Morel in Pediatric Research (1993)

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  2. Article

    PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY

    Prenatal diagnosis of the classic forms of the congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency has progressed at the same time as the advances made in the field of both endocrinology and ...

    Y Morel, M Murena, M G Forest, J C Carel, J Leger, J-L Nivelon… in Pediatric Research (1993)

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