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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| openAccess |  | 2011 | Cabimer (Centro Andaluz de Biología Molecular y Medicina Regenerativa) | Aguilera, Andrés CSIC ORCID; Bhattacharya, Shom Shanker CSIC ORCID; Soria Escoms, Bernat CSIC ORCID; Ríos, Rosa M. CSIC ORCID | presentación |
| openAccess |  | 2011 | Calendario 2012 Cabimer - Centro Andaluz de Biología Molecular y Medicina Regenerativa | Aguilera, Andrés CSIC ORCID; Bhattacharya, Shom Shanker CSIC ORCID; Soria Escoms, Bernat CSIC ORCID; Ríos, Rosa M. CSIC ORCID | presentación |
| closedAccess | | sep-1995 | cDNA Sequence and Gene Locus of the Human Retinal Phosphoinositide-Specific Phospholipase-Cβ4 (PLCB4) | Álvarez, Richard A.; Bhattacharya, Shom Shanker CSIC ORCID; Baehr, Wolfgang | artículo |
| closedAccess | | ago-2002 | Characterisation of two genes for guanylate cyclase activator protein (GCAP1 and GCAP2) in the Japanese pufferfish, Fugu rubripes | Wilkie, Susan E.; Bhattacharya, Shom Shanker CSIC ORCID; Hunt, David M. | artículo |
| closedAccess | | 2004 | Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract | Reddy, M.A.; Bhattacharya, Shom Shanker CSIC ORCID; Slingsby, C. | artículo |
| closedAccess | | oct-1999 | Characterization of the human diacylglycerol kinase e gene and its assessment as a candidate for inherited retinitis pigmentosa | Tang, Wen; Bardien, Soraya; Bhattacharya, Shom Shanker CSIC ORCID; Prescott, Stephen M. | artículo |
| closedAccess | | ago-2000 | Characterization of the Human TBX20 Gene, a New Member of the T-Box Gene Family Closely Related to the Drosophila H15 Gene | Meins, Moritz; Henderson, Deborah J.; Bhattacharya, Shom Shanker CSIC ORCID; Sowden, Jane C. | artículo |
| closedAccess | | nov-2000 | Chromosomal Duplication Involving the Forkhead Transcription Factor Gene FOXC1 Causes Iris Hypoplasia and Glaucoma | Lehmann, Ordan J.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| closedAccess |  | feb-1995 | Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype | Evans, Kevin; Duvall-Young, Josephine; Fitzke, Fred W.; Arden, Geoffrey B.; Bhattacharya, Shom Shanker CSIC ORCID; Bird, Alan C. | artículo |
| openAccess |  | 20-feb-2015 | Cleavage of mer tyrosine kinase (MerTK) from the cell surface contributes to the regulation of retinal phagocytosis | Law, Ah-Lai; Parinot, Célia; Chatagnon, Jonathan; Gravez, Basile; Sahel, José-Alain; Bhattacharya, Shom Shanker CSIC ORCID; Nandrot, Emeline F. | artículo |
| openAccess |  | 20-feb-2015 | Cleavage of mer tyrosine kinase (MerTK) from the cell surface contributes to the regulation of retinal phagocytosis | Law, Ah-Lai; Parinot, Célia; Chatagnon, Jonathan; Gravez, Basile; Sahel, José-Alain; Bhattacharya, Shom Shanker CSIC ORCID; Nandrot, Emeline F. | artículo |
| openAccess | ![ARTICULOS315483[1].pdf.jpg](/retrieve/1083131/ARTICULOS315483%5b1%5d.pdf.jpg) | 1999 | Clinical and genetic heterogeneity in autosomal dominant cataract | Ionides, Alexander; Bhattacharya, Shom Shanker CSIC ORCID; Moore, Anthony T. | artículo |
| openAccess | ![ARTICULOS315051[1].pdf.jpg](/retrieve/1082403/ARTICULOS315051%5b1%5d.pdf.jpg) | 2006 | Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene | Tschernutter, M.; Bhattacharya, Shom Shanker CSIC ORCID; Webster, Andrew R. | artículo |
| openAccess | ![ARTICULOS315090[1].pdf.jpg](/retrieve/1083133/ARTICULOS315090%5b1%5d.pdf.jpg) | ago-2005 | Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene | Aung, Tin; Bhattacharya, Shom Shanker CSIC ORCID; Hitchings, Roger A. | artículo |
| closedAccess | | mar-1998 | Clinical Features in Affected Individuals From 21 Pedigrees With Dominant Optic Atrophy | Votruba, Marcela; Bhattacharya, Shom Shanker CSIC ORCID; Moore, Anthony T. | artículo |
| closedAccess | | oct-1999 | Clinical Features of Codon 172 RDS Macular Dystrophy Similar Phenotype in 12 Families | Downes, Susan M.; Bhattacharya, Shom Shanker CSIC ORCID; Bird, Alan C. | artículo |
| closedAccess | | oct-1998 | Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy | Votruba, Marcela; Moore, Anthony T.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| closedAccess | | 13-nov-2002 | Cloning and characterization of WDR17, a novel WD repeat-containing gene on chromosome 4q34 | Stöhr, Heidi; Bhattacharya, Shom Shanker CSIC ORCID; Weber, Bernhard H.F. | artículo |
| closedAccess |  | 17-may-1984 | Close genetic linkage between X linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28 | Bhattacharya, Shom Shanker CSIC ORCID; Wright, Alan F.; Clayton, J. F.; Price, W. H.; Phillips, C. I.; McKeown, C. M. E.; Jay, Marcelle; Bird, Alan C.; Pearson, P. L.; Southern, E. M.; Evans, H. J. | artículo |
| closedAccess | | 2001 | Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies | Payne, Annette M.; Bhattacharya, Shom Shanker CSIC ORCID; Hunt, David M. | carta al director |
