1-3 of 3
Authors: François Kurtz
Sort by
Journal Article
The Prevalence of CHD7 Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients
Get access
Séverine Marcos and others
The Journal of Clinical Endocrinology & Metabolism, Volume 99, Issue 10, 1 October 2014, Pages E2138–E2143, https://doi.org/10.1210/jc.2014-2110
Published: 01 October 2014
Journal Article
Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients
Get access
Laurent Maimoun and others
The Journal of Clinical Endocrinology & Metabolism, Volume 96, Issue 2, 1 February 2011, Pages 296–307, https://doi.org/10.1210/jc.2010-1024
Published: 01 February 2011
Journal Article
Androgen Insensitivity Syndrome: Somatic Mosaicism of the Androgen Receptor in Seven Families and Consequences for Sex Assignment and Genetic Counseling
Get access
Birgit Köhler and others
The Journal of Clinical Endocrinology & Metabolism, Volume 90, Issue 1, 1 January 2005, Pages 106–111, https://doi.org/10.1210/jc.2004-0462
Published: 01 January 2005
Advertisement
Advertisement