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E Seemanova

Showing results (1-10 of 29) with videos related to

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La Radiologia Medica|April 3, 1998
Shprintzen-Goldberg syndrome. A case reportE Seemanova, K Kozlowski
Ceskoslovenska Pediatrie|March 1, 1970
[Typical hyperaminoaciduria and disulfiduria associated with mental retardation in an incest-born child]J Hyánek, E Seemanova, J Hoza
Cytogenetics and Cell Genetics|August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial caseO Bartsch, W Kress, A Wagner, et al.
Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.
Klinische Padiatrie|January 1, 1992
The Zimmermann-Laband syndromeR A Pfeiffer, E Seemanova, J Süss, et al.
European Journal of Neurology|December 23, 2004
Hypocretin deficiency in Prader-Willi syndromeS Nevsimalova, J Vankova, I Stepanova, et al.
Cancer Genetics and Cytogenetics|December 1, 1989
Ultraviolet-induced chromosomal instability in cultured fibroblasts of heterozygote carriers for xeroderma pigmentosumV Bielfeld, M Weichenthal, M Roser, et al.
Human Genetics|January 1, 1992
Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?K R Held, S Kerber, E Kaminsky, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Allelic heterogeneity of alkaptonuria in Central EuropeC R Müller, A Fregin, S Srsen, et al.
British Journal of Cancer|May 6, 1998
Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumoursZ Sedlacek, R Kodet, V Kriz, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
La Radiologia Medica|April 3, 1998
Shprintzen-Goldberg syndrome. A case reportE Seemanova, K Kozlowski
Ceskoslovenska Pediatrie|March 1, 1970
[Typical hyperaminoaciduria and disulfiduria associated with mental retardation in an incest-born child]J Hyánek, E Seemanova, J Hoza
Cytogenetics and Cell Genetics|August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial caseO Bartsch, W Kress, A Wagner, et al.
Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.
Klinische Padiatrie|January 1, 1992
The Zimmermann-Laband syndromeR A Pfeiffer, E Seemanova, J Süss, et al.
European Journal of Neurology|December 23, 2004
Hypocretin deficiency in Prader-Willi syndromeS Nevsimalova, J Vankova, I Stepanova, et al.
Cancer Genetics and Cytogenetics|December 1, 1989
Ultraviolet-induced chromosomal instability in cultured fibroblasts of heterozygote carriers for xeroderma pigmentosumV Bielfeld, M Weichenthal, M Roser, et al.
Human Genetics|January 1, 1992
Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?K R Held, S Kerber, E Kaminsky, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Allelic heterogeneity of alkaptonuria in Central EuropeC R Müller, A Fregin, S Srsen, et al.
British Journal of Cancer|May 6, 1998
Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumoursZ Sedlacek, R Kodet, V Kriz, et al.
Pageof 3