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H Forsius

Showing results (51-60 of 70) with videos related to

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Acta Ophthalmologica|January 1, 1973
Nystagmographical studies in Aland eye diseaseA G van Vliet, P J Waardenburg, H Forsius, et al.
Nordisk Medicin|December 3, 1970
[Qualitative and quantitative haptoglobin studies on the Finnish Lapps]A W Eriksson, M Kirjarinta, J Fellman, et al.
Genome Research|April 1, 1996
Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12E Tahvanainen, A S Villanueva, H Forsius, et al.
Acta Ophthalmologica|December 1, 1991
Clinical and electroretinographic comparison between Aland Island eye disease and a newly found related disease with X-chromosomal inheritanceS Carlson, E Vesti, C Raitta, et al.
Acta Ophthalmologica Scandinavica|May 20, 1998
Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in FinlandH Forsius, M Damsten, A W Eriksson, et al.
Clinical Genetics|June 1, 1980
Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinismF E O'Donnell, W R Green, V A McKusick, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in FinlandL Huopaniemi, A Rantala, H Forsius, et al.
American Journal of Human Genetics|January 1, 1991
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysisT Alitalo, T A Kruse, H Forsius, et al.
Journal of Medical Genetics|February 1, 1996
The genetics of cornea plana congenitaE Tahvanainen, H Forsius, J Kolehmainen, et al.
Clinical Genetics|May 1, 1987
Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidenceE M Sankila, A de la Chapelle, J Kärnä, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Acta Ophthalmologica|January 1, 1973
Nystagmographical studies in Aland eye diseaseA G van Vliet, P J Waardenburg, H Forsius, et al.
Nordisk Medicin|December 3, 1970
[Qualitative and quantitative haptoglobin studies on the Finnish Lapps]A W Eriksson, M Kirjarinta, J Fellman, et al.
Genome Research|April 1, 1996
Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12E Tahvanainen, A S Villanueva, H Forsius, et al.
Acta Ophthalmologica|December 1, 1991
Clinical and electroretinographic comparison between Aland Island eye disease and a newly found related disease with X-chromosomal inheritanceS Carlson, E Vesti, C Raitta, et al.
Acta Ophthalmologica Scandinavica|May 20, 1998
Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in FinlandH Forsius, M Damsten, A W Eriksson, et al.
Clinical Genetics|June 1, 1980
Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinismF E O'Donnell, W R Green, V A McKusick, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in FinlandL Huopaniemi, A Rantala, H Forsius, et al.
American Journal of Human Genetics|January 1, 1991
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysisT Alitalo, T A Kruse, H Forsius, et al.
Journal of Medical Genetics|February 1, 1996
The genetics of cornea plana congenitaE Tahvanainen, H Forsius, J Kolehmainen, et al.
Clinical Genetics|May 1, 1987
Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidenceE M Sankila, A de la Chapelle, J Kärnä, et al.
Pageof 7