Barto J. Otten

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

Dieter Kotzot, Silke Schmitt, Fabiana Bernasconi et al. · Human Molecular Genetics · 1995 · 302 citations · Full text

High Prevalence of Testicular Adrenal Rest Tumors, Impaired Spermatogenesis, and Leydig Cell Failure in Adolescent and Adult Males with Congenital Adrenal Hyperplasia

Nike Stikkelbroeck, Barto J. Otten, Arifa Pasic et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 294 citations

Spermatogenesis, Fertility, Gynecology +21

Final Height in Girls with Turner Syndrome after Long-Term Growth Hormone Treatment in Three Dosages and Low Dose Estrogens

Yvonne K. van Pareren, Sabine M.P.F. de Muinck Keizer‐Schrama, Theo Stijnen et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 241 citations · Full text

17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations1

Annemie L. M. Boehmer, Albert O. Brinkmann, Lodewijk A. Sandkuijl et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 177 citations · Full text

CYP21 Gene Mutation Analysis in 198 Patients with 21-Hydroxylase Deficiency in The Netherlands: Six Novel Mutations and a Specific Cluster of Four Mutations

Nike Stikkelbroeck, Lies H. Hoefsloot, Ilse J. de Wijs et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 170 citations · Full text

Specific Cluster, Mendelian Disorder, Congenital Adrenal Hyperplasia +14