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Showing results (101-110 of 156) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 6L Terrenato, C Jodice, P Blasi, et al.
Genomics|February 1, 1993
Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigreeG J Farrar, P Kenna, S A Jordan, et al.
Human Genetics|November 1, 1992
Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosaM Horn, P Humphries, M Kunisch, et al.
American Journal of Human Genetics|March 26, 1999
Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 geneF C Mansergh, S Millington-Ward, A Kennan, et al.
American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.
Journal of Medical Genetics|December 1, 1998
A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucomaA M Kennan, F C Mansergh, J H Fingert, et al.
Human Mutation|January 15, 1999
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindnessN al-Jandal, G J Farrar, A S Kiang, et al.
Plos One|August 1, 2023
Exploring the immune microenvironment in small bowel adenocarcinoma using digital image analysisFatima Abdullahi Sidi, Victoria Bingham, Stephen McQuaid, et al.
Nature|December 12, 1991
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosaG J Farrar, P Kenna, S A Jordan, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.
Pageof 16

Showing results (101-110 of 156) with videos related to

Sort By:
Pageof 16
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 6L Terrenato, C Jodice, P Blasi, et al.
Genomics|February 1, 1993
Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigreeG J Farrar, P Kenna, S A Jordan, et al.
Human Genetics|November 1, 1992
Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosaM Horn, P Humphries, M Kunisch, et al.
American Journal of Human Genetics|March 26, 1999
Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 geneF C Mansergh, S Millington-Ward, A Kennan, et al.
American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.
Journal of Medical Genetics|December 1, 1998
A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucomaA M Kennan, F C Mansergh, J H Fingert, et al.
Human Mutation|January 15, 1999
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindnessN al-Jandal, G J Farrar, A S Kiang, et al.
Plos One|August 1, 2023
Exploring the immune microenvironment in small bowel adenocarcinoma using digital image analysisFatima Abdullahi Sidi, Victoria Bingham, Stephen McQuaid, et al.
Nature|December 12, 1991
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosaG J Farrar, P Kenna, S A Jordan, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.
Pageof 16