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Navegación por Autor Bhattacharya, Shom Shanker

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DerechosPreviewFecha Public.TítuloAutor(es)Tipo
closedAccessaccesoRestringido.pdf.jpg29-ago-2012A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10qKamenarova, Kunka; Romero-Durán, Margarita CSIC; Valdés-Sánchez, María Lourdes; Bhattacharya, Shom Shanker CSIC ORCID; Chakarova, Christinaartículo
openAccessARTICULOS315469[1].pdf.jpgmar-2000A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13Hameed, Abdul; Bhattacharya, Shom Shanker CSIC ORCIDartículo
openAccessARTICULOS315056[1].pdf.jpgjul-2006A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic familyAddison, Peter K. F.; Bhattacharya, Shom Shanker CSIC ORCIDartículo
closedAccessmar-2006A study of the nuclear trafficking of the splicing factor protein PRPF31 linked to autosomal dominant retinitis pigmentosa (ADRP)Wilkie, Susan E.; Bhattacharya, Shom Shanker CSIC ORCID; Hunt, David M.artículo
closedAccessaccesoRestringido.pdf.jpg1994A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28Curtis, A. R.; Lindsay, S.; Boye, E.; Clarke, A. J.; Landy, S. J.; Bhattacharya, Shom Shanker CSIC ORCIDartículo
closedAccessago-1995A YAC Contig Spanning the Dominant Retinitis Pigmentosa Locus (RP9) on Chromosome 7pKeen, T. Jeffrey; Bhattacharya, Shom Shanker CSIC ORCIDartículo
openAccess1992Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutationMoore, Anthony T.; Fitzke, Fred W.; Kemp, Colin M.; Arden, Geoffrey B.; Keen, T. Jeffrey; Inglehearn, Christopher F.; Bhattacharya, Shom Shanker CSIC ORCID; Bird, Alan C.artículo
closedAccessdic-2000Abnormalities of the transforming growth factor-beta pathway in ocular melanomaMyatt, Nyree; Bhattacharya, Shom Shanker CSIC ORCID; Cree, Ian A.artículo
openAccessARTICULOS315736[1].pdf.jpgfeb-1993Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani familyCurtis, Ann; Bhattacharya, Shom Shanker CSIC ORCIDartículo
closedAccessaccesoRestringido.pdf.jpg1998Absence of p53 delays apoptotic photoreceptor cell death in the rds mouseAli, Robin R.; Reichel, Martin B.; Kanuga, Naheed; Munro, Peter M.; Alexander, Robert A.; Clarke, Alan R.; Luthert, Philip J.; Bhattacharya, Shom Shanker CSIC ORCID; Hunt, David M.artículo
closedAccessaccesoRestringido.pdf.jpg24-nov-1979Actual or standard bicarbonate?Tibi, Laila; Bhattacharya, Shom Shanker CSIC ORCID; Flear, Cecil T. G.carta al director
openAccessARTICULOS315565[1].pdf.jpgmar-2008Adeno-Associated Virus Gene Transfer to Mouse RetinaAli, Robin R.; Bhattacharya, Shom Shanker CSIC ORCID; Thrasher, Adrián J.artículo
closedAccess2001Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in HumansBerry, Vanita; Bhattacharya, Shom Shanker CSIC ORCID; Quinlan, Roy A.artículo
openAccessARTICULOS315470[1].pdf.jpgene-2000An Analysis of ABCR Mutations in British Patients with Recessive Retinal DystrophiesPapaioannou, Myrto G.; Bhattacharya, Shom Shanker CSIC ORCIDartículo
openAccessARTICULOS315036[1].pdf.jpgdic-2007An Assessment of the Apex Microarray Technology in Genotyping Patients with Leber Congenital Amaurosis and Early-Onset Severe Retinal DystrophyHenderson, Robert H.; Bhattacharya, Shom Shanker CSIC ORCID; Moore, Anthony T.artículo
closedAccessaccesoRestringido.pdf.jpg1-ago-1995An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17qBardien, Soraya; Ebenezer, Neil D.; Greenberg, Jacquie; Inglehearn, Christopher F.; Bartmann, Lecia; Goliath, Rene; Beighton, Peter; Ramesar, Rajkumar; Bhattacharya, Shom Shanker CSIC ORCIDartículo
openAccessARTICULOS315436[1].pdf.jpg2001An immune response after intraocular administration of an adenoviral vector containing a β galactosidase reporter gene slows retinal degeneration in the rd mouseReichel, Martin B.; Bhattacharya, Shom Shanker CSIC ORCID; Ali, Robin R.artículo
closedAccessabr-2002An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic DisordersThiselton, Dawn L.; Bhattacharya, Shom Shanker CSIC ORCID; Meindl, Alfonsartículo
closedAccessaccesoRestringido.pdf.jpg1-mar-1998Anterior polar cataract: clinical spectrum and genetic linkage in a single familyIonides, Alexander; Berry, Vanita; Mackay, Donna; Shiels, Alan; Bhattacharya, Shom Shanker CSIC ORCID; Moore, Anthony T.artículo
closedAccessaccesoRestringido.pdf.jpg2001Assignment (1) of BCL2L11 to human chromosome band 2p13 with somatic cell and radiation hybridsMurray, S.; Halford, S.; Ebenezer, Neil D.; Gregory-Evans, Cheryl Y.; Bhattacharya, Shom Shanker CSIC ORCIDartículo