Authors:
Deneux, C
Tardy, V
Dib, A
Mornet, E
Billaud, L
Charron, D
Morel, Y
Kuttenn, F
Citation: C. Deneux et al., Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency, J CLIN END, 86(1), 2001, pp. 207-213
Authors:
Simard, J
Ricketts, AL
Moisan, AM
Tardy, V
Peter, M
Van Vliet, G
Morel, Y
Citation: J. Simard et al., A new insight into the molecular basis of 3 beta-hydroxysteroid dehydrogenase deficiency, ENDOCRINE R, 26(4), 2000, pp. 761-770
Authors:
Delague, V
Souraty, N
Khallouf, E
Tardy, V
Chouery, E
Halaby, G
Loiselet, J
Morel, Y
Megarbane, A
Citation: V. Delague et al., Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylase, HORMONE RES, 53(2), 2000, pp. 77-82
Authors:
L'Allemand, D
Tardy, V
Gruters, A
Schnabel, D
Krude, H
Morel, Y
Citation: D. L'Allemand et al., 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, J CLIN END, 85(12), 2000, pp. 4562-4567
Authors:
Moisan, AM
Ricketts, ML
Tardy, V
Desrochers, M
Mebarki, F
Chaussain, JL
Cabrol, S
Raux-Demay, MC
Forest, MG
Sippell, WG
Peter, M
Morel, Y
Simard, J
Citation: Am. Moisan et al., Commentary - New insight into the molecular basis of 3 beta-hydroxysteroiddehydrogenase deficiency: Identification of fight mutations in the HSD3B2 gene in eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes, J CLIN END, 84(12), 1999, pp. 4410-4425