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K O Simola

Showing results (11-20 of 25) with videos related to

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Journal of Medical Genetics|September 1, 1995
Clinical features of nine males with molecularly defined deletions of the Y chromosome long armP Salo, J Ignatius, K O Simola, et al.
Human Genetics|January 1, 1983
Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumorK O Simola, S Knuutila, I Kaitila, et al.
The Laryngoscope|June 1, 1995
Usher's syndrome type 3 in FinlandL Pakarinen, S Karjalainen, K O Simola, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1993
[Incidence of Down syndrome and prenatal diagnosis during the years 1984-88 in Finland]R Salonen, K O Simola, T Harjulehto-Mervaala, et al.
American Journal of Medical Genetics|February 15, 1994
X-linked laterality sequence in a family with carrier manifestationsS P Mikkilä, M Janas, R Karikoski, et al.
Somatic Cell and Molecular Genetics|November 1, 1989
Long-range restriction map around 11p13 aniridia locusL M Davis, A M Everest, K O Simola, 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.
Human Genetics|December 1, 1986
Localization of the LDHA gene to 11p14----11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13T L Yang-Feng, G A Bruns, A J Carroll, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1985
[Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics]M Lindlöf, P Ammälä, H Somer, et al.
Prenatal Diagnosis|November 14, 1997
Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1A Mustonen, H K Ploos van Amstel, R Berger, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|September 1, 1995
Clinical features of nine males with molecularly defined deletions of the Y chromosome long armP Salo, J Ignatius, K O Simola, et al.
Human Genetics|January 1, 1983
Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumorK O Simola, S Knuutila, I Kaitila, et al.
The Laryngoscope|June 1, 1995
Usher's syndrome type 3 in FinlandL Pakarinen, S Karjalainen, K O Simola, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1993
[Incidence of Down syndrome and prenatal diagnosis during the years 1984-88 in Finland]R Salonen, K O Simola, T Harjulehto-Mervaala, et al.
American Journal of Medical Genetics|February 15, 1994
X-linked laterality sequence in a family with carrier manifestationsS P Mikkilä, M Janas, R Karikoski, et al.
Somatic Cell and Molecular Genetics|November 1, 1989
Long-range restriction map around 11p13 aniridia locusL M Davis, A M Everest, K O Simola, 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.
Human Genetics|December 1, 1986
Localization of the LDHA gene to 11p14----11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13T L Yang-Feng, G A Bruns, A J Carroll, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1985
[Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics]M Lindlöf, P Ammälä, H Somer, et al.
Prenatal Diagnosis|November 14, 1997
Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1A Mustonen, H K Ploos van Amstel, R Berger, et al.
Pageof 3