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Journal Articles

Three Novel CYP11B1 Mutations in Congenital Adrenal Hyperplasia due to Steroid 11Beta-Hydroxylase Deficiency in a Moroccan Population

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Subject Area:
Endocrinology , Women's and Children's Health
L. Chabraoui, F. Abid, R. Menassa, A. Gaouzi, A. El Hessni, Y. Morel
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2010) 74 (3): 182–189.
https://doi.org/10.1159/000281417
Published Online: 03 June 2010
View articletitled, Three Novel CYP11B1 Mutations in Congenital Adrenal Hyperplasia due to Steroid 11Beta-Hydroxylase Deficiency in a Moroccan Population
Open the PDF for Three Novel CYP11B1 Mutations in Congenital Adrenal Hyperplasia due to Steroid 11Beta-Hydroxylase Deficiency in a Moroccan Population in another window
Journal Articles

Cosegregation of a Novel Homozygous CYP11B1 Mutation with the Phenotype of Non-Classical Congenital Adrenal Hyperplasia in a Consanguineous Family

Available to Purchase
Subject Area:
Endocrinology , Women's and Children's Health
C.J. Peters, T. Nugent, L.A. Perry, K. Davies, Y. Morel, W.M. Drake, M.O. Savage, L.B. Johnston
Journal: Hormone Research in Paediatrics
Hormone Research (2007) 67 (4): 189–193.
https://doi.org/10.1159/000097244
Published Online: 20 November 2006
View articletitled, Cosegregation of a Novel Homozygous CYP11B1 Mutation with the Phenotype of Non-Classical Congenital Adrenal Hyperplasia in a Consanguineous Family
Open the PDF for Cosegregation of a Novel Homozygous CYP11B1 Mutation with the Phenotype of Non-Classical Congenital Adrenal Hyperplasia in a Consanguineous Family in another window