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Marjatta Sipponen

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Orphanet Journal of Rare Diseases|June 23, 2011
9q22 Deletion--first familial caseLinda Siggberg, Maarit Peippo, Marjatta Sipponen, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
PAK3 related mental disability: further characterization of the phenotypeMaarit Peippo, Anne M Koivisto, Teppo Särkämö, et al.
American Journal of Human Genetics|February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationGuy Froyen, Mark Corbett, Joke Vandewalle, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Orphanet Journal of Rare Diseases|June 23, 2011
9q22 Deletion--first familial caseLinda Siggberg, Maarit Peippo, Marjatta Sipponen, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
PAK3 related mental disability: further characterization of the phenotypeMaarit Peippo, Anne M Koivisto, Teppo Särkämö, et al.
American Journal of Human Genetics|February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationGuy Froyen, Mark Corbett, Joke Vandewalle, et al.
Pageof 1