Hans J. van der Harten

Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

Andrea Superti‐Furga, Johanna Hästbacka, William R. Wilcox et al. · Nature Genetics · 1996 · 234 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

A Frame-Shift Mutation in the Type I Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Causing Blomstrand Lethal Osteochondrodysplasia

Marcel Karperien, Hans J. van der Harten, Ron van Schooten et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 86 citations · Full text

Ultrasonographic and radiologic visualization of the developing embryonic skeleton

R. M. Van Zalen‐Sprock, Jozien T. J. Brons, J. M. G. van Vugt et al. · Ultrasound in Obstetrics and Gynecology · 1997 · 76 citations

Phenotypic and genotypic overlap between atelosteogenesis type 2 and diastrophic dysplasia

Antonio Rossi, Hans J. van der Harten, Frits A. Beemer et al. · Human Genetics · 1996 · 59 citations

Developmental Anomaly, Developmental Biology, Diastrophic Dysplasia +6

Prenatal ultrasonographic diagnosis of osteogenesis imperfecta

Jozien T. J. Brons, Hans J. van der Harten, Juri W. Wladimiroff et al. · American Journal of Obstetrics and Gynecology · 1988 · 56 citations

Bone Imaging, Pediatrics, Osteogenesis +6