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Experimental and Clinical Immunogenetics|July 8, 1999
Five new polymorphisms in the complement C7 gene and their association with C7 deficiencyB A Fernie, M J HobartCritical Care Clinics|July 1, 1992
Ten years of maternal-fetal transportC Ackmann, G Russano, J HobartJournal of Pediatric Rehabilitation Medicine|March 17, 2025
Sleep-related breathing disorders in children with spina bifidaKiran Nandalike, Laura J Hobart-PorterCiba Foundation Symposium|June 27, 1979
The genetics of the complement systemP J Lachmann, M J HobartHuman Genetics|December 18, 1998
Complement C7 deficiency: seven further molecular defects and their associated marker haplotypesB A Fernie, M J HobartJournal of Youth and Adolescence|November 27, 2013
Maternal regulation and adolescent autonomy: Mother-daughter resolution of story conflictsJ Hakim-Larson, C J HobartHuman Genetics|July 1, 1997
An unusual combined insertion/deletion polymorphism in intron 10 of the human complement C6 geneB A Fernie, M J HobartJournal of Neurology|January 22, 2008
Testing the SF-36 in Parkinson's disease. Implications for reporting rating scale dataP Hagell, A L Törnqvist, J HobartClinical and Experimental Immunology|August 1, 1978
Combined genetic deficiency of C6 and C7 in manP J Lachmann, M J Hobart, P WooExperimental Neurology|January 8, 1999
Transplanted neurons alter the course of neurodegenerative disease in Lurcher mutant miceJ A Heckroth, N J Hobart, D SummersPageof 594