Wolfram Henn

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran et al. · The American Journal of Human Genetics · 2005 · 277 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

Heike Starke, Jörg Seidel, Wolfram Henn et al. · European Journal of Human Genetics · 2002 · 204 citations

Life Sciences, Genetics, Molecular Genetics +13

Mutations in the<i>UBIAD1</i>Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy

Jayne S. Weiss, Howard S. Kruth, Helena Kuivaniemi et al. · Investigative Ophthalmology & Visual Science · 2007 · 104 citations

Medicine, Genetics, Ophthalmology +17

Deletion of chromosome 1p and loss of expression of alkaline phosphatase indicate progression of meningiomas.

Patrick Müller, Wolfram Henn, I. Niedermayer et al. · PubMed · 1999 · 95 citations

Life Sciences, Oncology, Pathology +13

Malignant odontogenic myxoma of the maxilla: case with cytogenetic confirmation

Stefan Pahl, Wolfram Henn, Thomas Binger et al. · The Journal of Laryngology & Otology · 2000 · 59 citations

Veterinary Medicine, Oncology, Oral Pathology +17