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American Journal of Medical Genetics|October 6, 1999
Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: bent but not brokenR M Pauli, P Modaff, S L Sipes, et al.American Journal of Medical Genetics|January 2, 1995
Natural history study of hereditary multiple exostosesC L Wicklund, R M Pauli, D Johnston, et al.American Journal of Medical Genetics|April 1, 1983
Familial agnathia-holoprosencephalyR M Pauli, J C Pettersen, S Arya, et al.British Journal of Audiology|November 1, 1978
A theoretical approach to the loop induction systemR M Barr-HamiltonJournal of Intellectual Disability Research : JIDR|May 11, 2011
Identifying the barriers and facilitators to participation in physical activity for children with Down syndromeM Barr, N ShieldsAmerican Journal of Human Genetics|October 1, 1987
Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivativesR M Pauli, J B Lian, D F Mosher, et al.Clinical Genetics|September 1, 1991
Absence of predictable phenotypic expression in proximal 15q duplicationsC J Ludowese, K J Thompson, G S Sekhon, et al.Pageof 119