Jan J. M. de Vijlder

Maternal-Fetal Transfer of Thyroxine in Congenital Hypothyroidism Due to a Total Organification Defect or Thyroid Agenesis

Thomas Vulsma, Margareth H. Gons, Jan J. M. de Vijlder · New England Journal of Medicine · 1989 · 803 citations

Inactivating Mutations in the Gene for Thyroid Oxidase 2 (<i>THOX2</i>) and Congenital Hypothyroidism

J.C. Moreno, Hennie Bikker, Marlies Kempers et al. · New England Journal of Medicine · 2002 · 474 citations · Full text

Effects of Thyroxine Supplementation on Neurologic Development in Infants Born at Less Than 30 Weeks' Gestation

Aleid G. van Wassenaer, Joke H. Kok, Jan J. M. de Vijlder et al. · New England Journal of Medicine · 1997 · 295 citations · Full text

Two Frequent Missense Mutations in Pendred Syndrome

Peter Van Hauwe, Lorraine A. Everett, Paul Coucke et al. · Human Molecular Genetics · 1998 · 189 citations · Full text

Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update)

Hennie Bikker, Thomas Vulsma, Janine S. E. de Randamie et al. · The Journal of Clinical Endocrinology & Metabolism · 2000 · 182 citations

Mendelian Disorder, Exon 9, Genetic Disorder +13