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Cytogenetics and Cell Genetics|January 1, 1995
X-linked juvenile retinoschisis (RS) maps between DXS987 and DXS443B H Weber, S Janocha, G Vogt, et al.Nature Genetics|June 1, 1994
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qterB H Weber, G Vogt, W Wolz, et al.American Journal of Human Genetics|December 1, 1994
High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11B H Weber, G Vogt, H Stöhr, et al.Nature Genetics|November 5, 1997
Positional cloning of the gene associated with X-linked juvenile retinoschisisC G Sauer, A Gehrig, R Warneke-Wittstock, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 2, 1998
The natural history of X-linked retinoschisisM T Roesch, C C Ewing, A E Gibson, et al.Nature Genetics|December 1, 1994
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyB H Weber, G Vogt, R C Pruett, et al.The British Journal of Ophthalmology|August 1, 1996
Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of casesB H Weber, S Sander, C Kopp, et al.Physiology & Behavior|September 27, 2005
Effects of selective estrogen receptor agonists on food intake and body weight gain in ratsDarren M RoeschJournal of Dental Education|January 4, 2014
Temporally contiguous pencast instruction promotes meaningful learning for dental and dental hygiene students in physiologyDarren M RoeschActa Anatomica|December 1, 1998
Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the maculaB H WeberPageof 219