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R J Patel

Showing results (21-30 of 34) with videos related to

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Journal of Clinical Psychology|May 1, 1995
Hopelessness predicts future depressive symptoms: a prospective analysis of cognitive vulnerability and cognitive content specificityB A Alford, J M Lester, R J Patel, et al.
Genomics|January 20, 1995
Localization of the aquaporin 1 (AQP1) gene within a YAC contig containing the polymorphic markers D7S632 and D7S526T J Keen, C F Inglehearn, R J Patel, et al.
Minerva Cardioangiologica|August 4, 2012
Emerging oral anticoagulants for stroke prevention in patients with non-valvular atrial fibrillationC Destephan, A H Waller, R J Patel, et al.
Chemosphere|December 21, 2025
A national-scale preliminary overview study of poly- and perfluoroalkyl substances (PFAS) occurrence in aquatic environments of England, UKR J Patel, D C Gooddy, B Marchant, et al.
Chemosphere|March 11, 2026
Corrigendum to 'A national-scale preliminary overview study of poly- and perfluoroalkyl substances (PFAS) occurrence in aquatic environments of England, UK' [Chemosphere 394 (2026) 144804]R J Patel, D C Gooddy, B Marchant, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 15, 2000
Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis geneJ H Park, S H Ott, X Wang, et al.
Genomics|November 1, 1995
Regional assignment of 30 expressed sequence tags on human chromosome 7 using a somatic cell hybrid panelR J Patel, T J Keen, K H Grzeschik, et al.
Molecular Biology Reports|July 18, 2001
Isolation and characterization of the human homeobox gene HOX D1B Appukuttan, R Sood, S Ott, et al.
The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.
The British Journal of Ophthalmology|November 12, 2003
Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessL E Allen, I Zito, K Bradshaw, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Journal of Clinical Psychology|May 1, 1995
Hopelessness predicts future depressive symptoms: a prospective analysis of cognitive vulnerability and cognitive content specificityB A Alford, J M Lester, R J Patel, et al.
Genomics|January 20, 1995
Localization of the aquaporin 1 (AQP1) gene within a YAC contig containing the polymorphic markers D7S632 and D7S526T J Keen, C F Inglehearn, R J Patel, et al.
Minerva Cardioangiologica|August 4, 2012
Emerging oral anticoagulants for stroke prevention in patients with non-valvular atrial fibrillationC Destephan, A H Waller, R J Patel, et al.
Chemosphere|December 21, 2025
A national-scale preliminary overview study of poly- and perfluoroalkyl substances (PFAS) occurrence in aquatic environments of England, UKR J Patel, D C Gooddy, B Marchant, et al.
Chemosphere|March 11, 2026
Corrigendum to 'A national-scale preliminary overview study of poly- and perfluoroalkyl substances (PFAS) occurrence in aquatic environments of England, UK' [Chemosphere 394 (2026) 144804]R J Patel, D C Gooddy, B Marchant, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 15, 2000
Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis geneJ H Park, S H Ott, X Wang, et al.
Genomics|November 1, 1995
Regional assignment of 30 expressed sequence tags on human chromosome 7 using a somatic cell hybrid panelR J Patel, T J Keen, K H Grzeschik, et al.
Molecular Biology Reports|July 18, 2001
Isolation and characterization of the human homeobox gene HOX D1B Appukuttan, R Sood, S Ott, et al.
The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.
The British Journal of Ophthalmology|November 12, 2003
Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessL E Allen, I Zito, K Bradshaw, et al.
Pageof 4