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H Forsius

Showing results (61-70 of 70) with videos related to

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Annals of Human Genetics|March 14, 2001
Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 geneL Huopaniemi, J Fellman, A Rantala, et al.
Acta Ophthalmologica|August 1, 1983
Granular corneal dystrophy with late manifestationH Forsius, A W Eriksson, J Kărnă, et al.
Genomics|March 20, 1995
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysisE Tahvanainen, H Forsius, E Karila, et al.
Genomics|December 10, 1995
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2E Tahvanainen, H Forsius, M Damsten, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 1, 1973
Visual acuity in 183 cases of X-chromosomal retinoschisisH Forsius, U Krause, J Helve, et al.
The British Journal of Ophthalmology|June 21, 2005
Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 geneL Lauronen, R Jalkanen, J Huttunen, et al.
American Journal of Human Genetics|October 1, 1988
Linkage relationships and gene order around the locus for X-linked retinoschisisT Alitalo, H Forsius, J Kärnä, et al.
Human Genetics|December 1, 1989
Haplotype and multipoint linkage analysis in Finnish choroideremia familiesE M Sankila, T Lehner, A W Eriksson, et al.
Investigative Ophthalmology & Visual Science|July 13, 2000
Autosomal recessive cornea plana: in vivo corneal morphology and corneal sensitivityM H Vesaluoma, E M Sankila, J Gallar, et al.
Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Annals of Human Genetics|March 14, 2001
Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 geneL Huopaniemi, J Fellman, A Rantala, et al.
Acta Ophthalmologica|August 1, 1983
Granular corneal dystrophy with late manifestationH Forsius, A W Eriksson, J Kărnă, et al.
Genomics|March 20, 1995
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysisE Tahvanainen, H Forsius, E Karila, et al.
Genomics|December 10, 1995
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2E Tahvanainen, H Forsius, M Damsten, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 1, 1973
Visual acuity in 183 cases of X-chromosomal retinoschisisH Forsius, U Krause, J Helve, et al.
The British Journal of Ophthalmology|June 21, 2005
Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 geneL Lauronen, R Jalkanen, J Huttunen, et al.
American Journal of Human Genetics|October 1, 1988
Linkage relationships and gene order around the locus for X-linked retinoschisisT Alitalo, H Forsius, J Kärnä, et al.
Human Genetics|December 1, 1989
Haplotype and multipoint linkage analysis in Finnish choroideremia familiesE M Sankila, T Lehner, A W Eriksson, et al.
Investigative Ophthalmology & Visual Science|July 13, 2000
Autosomal recessive cornea plana: in vivo corneal morphology and corneal sensitivityM H Vesaluoma, E M Sankila, J Gallar, et al.
Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.
Pageof 7