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Journal of Pediatric Gastroenterology and Nutrition|February 1, 1992
Detection of hepatitis B virus DNA in the liver of children with chronic hepatitis B by in situ hybridization and its relation to other viral markersS Wirth, A Hueter, I Blaha, et al.Archives of Dermatological Research|January 1, 1994
Ehlers-Danlos syndrome type VII: phenotype and genotypeH W Lehmann, S Mundlos, A Winterpacht, et al.Development (Cambridge, England)|November 1, 1992
PAX8, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms' tumorsA Poleev, H Fickenscher, S Mundlos, et al.Journal of Medical Genetics|April 16, 1999
Cleidocranial dysplasia: clinical and molecular geneticsS MundlosNovartis Foundation Symposium|March 30, 2001
Defects of human skeletogenesis--models and mechanismsS MundlosMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1989
[Gene therapy]B ZabelAmerican Journal of Human Genetics|June 23, 1998
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9S G Kant, A Polinkovsky, S Mundlos, et al.Current Opinion in Rheumatology|October 1, 1991
Genetic disorders of connective tissuesS Mundlos, J SprangerFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 1, 1997
Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasisS Mundlos, B R OlsenPageof 18