Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Ebenezer, Neil"'
Autor:
Ebenezer, Neil, Dalkmann, Holger, Haq, Gary, Cervantes Barron, Karla, Brand, Christian, Dixon, James, Collett, Katherine, Cullen, Jon, Hine, John, Hirmer, Stephanie, Patterson, Simon, Pye, Steve, Sivakumar, Aruna, Welsby, Daniel
This discussion paper, is the result of an overall effort undertaken by the Sustainable Mobility for All partnership, in conjunction with the UK Foreign, Commonwealth and Development Office (FCDO) and the Climate Compatible Growth (CCG) Programme. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0bb7bebbc63dba7d624f29f7cb878a
https://ora.ox.ac.uk/objects/uuid:1f4f989f-4d90-415a-99cf-8aa3ccfe89db
https://ora.ox.ac.uk/objects/uuid:1f4f989f-4d90-415a-99cf-8aa3ccfe89db
Autor:
Jirsova, Katerina, Merjava, Stanislava, Martincova, Radka, Gwilliam, Rhian, Ebenezer, Neil D., Liskova, Petra, Filipec, Martin
Publikováno v:
In Experimental Eye Research 2007 84(4):680-686
Autor:
Brooks, Simon P.1, Ebenezer, Neil D.1, Poopalasundaram, Subathra1, Maher, Eamonn R.2, Francis, Peter J.1,3, Moore, Anthony T.1,3, Hardcastle, Alison J.1 a.hardcastle@ucl.ac.uk
Publikováno v:
Ophthalmic Genetics. Jun2004, Vol. 25 Issue 2, p121-131. 11p. 3 Diagrams, 3 Charts.
Autor:
Davidson, Alice E, Liskova, Petra, Evans, Cerys J, Dudakova, Lubica, Noskova, Lenka, Pontikos, Nikolas, Hartmannova, Hana, Hodanova, Katerina, Stranecky, Viktor, Kozmik, Zbynek, Levis, Hannah J, Idigo, Nwamaka, Sasai, Noriaki, Maher, Geoffrey J, Bellingham, James, Veli, Neyme, Ebenezer, Neil D, Cheetham, Michael E, Daniels, Julie T, Thaung, Caroline MH, Jirsova, Katerina, Plagnol, Vincent, Filipec, Martin, Kmoch, Stanislav, Tuft, Stephen J, Hardcastle, Alison J
Publikováno v:
AMERICAN JOURNAL OF HUMAN GENETICS
Congenital hereditary endothelial dystrophy 1 (CHED1) and posterior polymorphous corneal dystrophy 1 (PPCD1) are autosomal-dominant corneal endothelial dystrophies that have been genetically mapped to overlapping loci on the short arm of chromosome 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::90350a0656ece1e03a7f2ff3437ae849
https://doi.org/10.1016/j.ajhg.2015.11.018
https://doi.org/10.1016/j.ajhg.2015.11.018
Akademický článek
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Autor:
Lehmann, Ordan J., El-Ashry, Mohamed F., Ebenezer, Neil D., Ocaka, Louise, Francis, Peter J., Wilkie, Susan E., Patel, Reshma J., Ficker, Linda, Jordan, Tim, Khaw, Peng T., Bhattacharya, Shom Shanker
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
PURPOSE: Mutations in keratocan (KERA), a small leucine-rich proteoglycan, have recently been shown to be responsible for cases of autosomal recessive cornea plana (CNA2). A consanguineous pedigree in which cornea plana cosegregated with microphthalm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::baaa37e82d68d7882af056cf60849a5a
http://hdl.handle.net/10261/270410
http://hdl.handle.net/10261/270410
Autor:
Murray, S., Halford, S., Ebenezer, Neil D., Gregory-Evans, Cheryl Y., Bhattacharya, Shom Shanker
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::020c1a8cde4e6700f175394f2df3046c
http://hdl.handle.net/10261/270468
http://hdl.handle.net/10261/270468
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Gardner, Jessica C., Webb, Tom R., Kanuga, Naheed, Robson, Anthony G., Holder, Graham E., Stockman, Andrew, Ripamonti, Caterina, Ebenezer, Neil D., Ogun, Olufunmilola, Devery, Sophie, Wright, Genevieve A., Maher, Eamonn R., Cheetham, Michael E., Moore, Anthony T., Michaelides, Michel, Hardcastle, Alison J.
Publikováno v:
Retinal Degenerative Diseases (9781461406303); 2012, p595-601, 7p