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Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
American Journal of Human Genetics|April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)C F Inglehearn, T J Keen, M al-Maghtheh, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|October 10, 2013
Association between maternal body mass index during pregnancy, short-term morbidity, and increased health service costs: a population-based studyF C Denison, P Norwood, S Bhattacharya, et al.
Human Genetics|March 10, 1999
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)S Kermani, K Gregory-Evans, E E Tarttelin, et al.
British Journal of Obstetrics and Gynaecology|May 1, 1997
A pragmatic randomised comparison of transcervical resection of the endometrium with endometrial laser ablation for the treatment of menorrhagiaS Bhattacharya, I M Cameron, D E Parkin, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Single exposures to antiproliferatives: long-term effects on ocular fibroblast wound-healing behaviorN L Occleston, J T Daniels, R W Tarnuzzer, et al.
Nature Communications|August 26, 2018
High entropy oxides for reversible energy storageAbhishek Sarkar, Leonardo Velasco, Di Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity testsJ Ott, S Bhattacharya, J D Chen, et al.
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