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Navegación por Autor Ebenezer, Neil D.
Mostrando resultados 1 a 6 de 6
| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| closedAccess |  | 2005 | A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in british population | El-Ashry, Mohamed F.; Abd El-Aziz, Mai M.; Hardcastle, Alison; Bhattacharya, Shom Shanker CSIC ORCID; Ebenezer, Neil D. | artículo |
| openAccess | ![ARTICULOS315265[1].pdf.jpg](/retrieve/1082162/ARTICULOS315265%5b1%5d.pdf.jpg) | jul-2003 | A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British families | El-Ashry, Mohamed F.; Bhattacharya, Shom Shanker CSIC ORCID; Ebenezer, Neil D. | artículo |
| closedAccess |  | dic-2001 | A Novel Keratocan Mutation Causing Autosomal Recessive Cornea Plana | 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 CSIC ORCID | artículo |
| closedAccess |  | 1-ago-1995 | An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q | Bardien, Soraya; Ebenezer, Neil D.; Greenberg, Jacquie; Inglehearn, Christopher F.; Bartmann, Lecia; Goliath, Rene; Beighton, Peter; Ramesar, Rajkumar; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| closedAccess |  | 2001 | Assignment (1) of BCL2L11 to human chromosome band 2p13 with somatic cell and radiation hybrids | Murray, S.; Halford, S.; Ebenezer, Neil D.; Gregory-Evans, Cheryl Y.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| closedAccess | | 2004 | BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI | El-Ashry, Mohamed F.; Bhattacharya, Shom Shanker CSIC ORCID; Ebenezer, Neil D. | artículo |
