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E M Sankila

Showing results (1-10 of 28) with videos related to

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Clinical Genetics|March 1, 1993
Attitudes towards prenatal diagnosis and selective abortion among patients with retinitis pigmentosa or choroideremia as well as among their relativesT Furu, H Kääriäinen, E M Sankila, et al.
Human Genetics|July 1, 1991
Choroideremia: linkage analysis with physically mapped close DNA-markersE M Sankila, P Sistonen, F Cremers, et al.
Clinical Genetics|October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosisA de la Chapelle, E M Sankila, M Lindlöf, et al.
American Journal of Human Genetics|May 1, 1985
Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1)A E Vauhkonen, E M Sankila, K O Simola, et al.
Genomics|March 8, 2000
A sequence-ready map of the Usher syndrome type III critical region on chromosome 3qT Joensuu, R Hämäläinen, A E Lehesjoki, et al.
Journal of Medical Genetics|May 23, 1998
Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanismS Ala-Mello, E M Sankila, O Koskimies, 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.
Ophthalmology|May 18, 1999
In vivo confocal microscopy of a family with Schnyder crystalline corneal dystrophyM H Vesaluoma, T U Linna, E M Sankila, et al.
Genomics|December 15, 1996
Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous regionT Joensuu, G Blanco, L Pakarinen, et al.
Human Molecular Genetics|January 1, 1995
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3qE M Sankila, L Pakarinen, H Kääriäinen, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Clinical Genetics|March 1, 1993
Attitudes towards prenatal diagnosis and selective abortion among patients with retinitis pigmentosa or choroideremia as well as among their relativesT Furu, H Kääriäinen, E M Sankila, et al.
Human Genetics|July 1, 1991
Choroideremia: linkage analysis with physically mapped close DNA-markersE M Sankila, P Sistonen, F Cremers, et al.
Clinical Genetics|October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosisA de la Chapelle, E M Sankila, M Lindlöf, et al.
American Journal of Human Genetics|May 1, 1985
Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1)A E Vauhkonen, E M Sankila, K O Simola, et al.
Genomics|March 8, 2000
A sequence-ready map of the Usher syndrome type III critical region on chromosome 3qT Joensuu, R Hämäläinen, A E Lehesjoki, et al.
Journal of Medical Genetics|May 23, 1998
Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanismS Ala-Mello, E M Sankila, O Koskimies, 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.
Ophthalmology|May 18, 1999
In vivo confocal microscopy of a family with Schnyder crystalline corneal dystrophyM H Vesaluoma, T U Linna, E M Sankila, et al.
Genomics|December 15, 1996
Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous regionT Joensuu, G Blanco, L Pakarinen, et al.
Human Molecular Genetics|January 1, 1995
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3qE M Sankila, L Pakarinen, H Kääriäinen, et al.
Pageof 3