P J Willems

Nonsyndromic hearing impairment: unparalleled heterogeneity.

Guy Van Camp, P J Willems, Richard J. Smith · PubMed · 1997 · 336 citations

Medicine, Audiology, Otolaryngology +12

Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

Karin Buiting, Bärbel Dittrich, Stephanie Groß et al. · The American Journal of Human Genetics · 1998 · 216 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

Wim Wuyts, Wim Van Hul, Kristel De Boulle et al. · The American Journal of Human Genetics · 1998 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Sonya I. Haslam, Wim Van Hul, Antonio Morales‐Piga et al. · Journal of Bone and Mineral Research · 1998 · 141 citations · Full text

Medicine, Genetics, Molecular Genetics +17

cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.

Jutta Davidson, C Hamacher, P J Willems et al. · Proceedings of the National Academy of Sciences · 1992 · 94 citations

Life Sciences, Genetics, Molecular Genetics +12