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Marja Hietala

Showing results (1-10 of 33) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|August 7, 2015
[Parkinson's disease associated with a mutation in the PARK2 gene]Valtteri Kaasinen, Marja Hietala, Mikko Kuoppamäki
New Genetics and Society|October 9, 2004
Ethical issues in the diagnostic genetic testing processTarja Nyrhinen, Helena Leino-Kilpi, Marja Hietala
Clinical and Translational Allergy|June 27, 2017
Food allergy in a child with de novo <i>KAT6A</i> mutationVarpu Elenius, Tuire Lähdesmäki, Marja Hietala, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
A 69-year-old woman with Coffin-Siris syndromeLaura Määttänen, Marja Hietala, Jaakko Ignatius, et al.
Nursing Ethics|April 27, 2007
Privacy and equality in diagnostic genetic testingTarja Nyrhinen, Marja Hietala, Pauli Puukka, et al.
Neurology. Genetics|April 12, 2016
Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutationMika H Martikainen, Markku Päivärinta, Marja Hietala, et al.
Journal of Genetic Counseling|November 4, 2008
Are patient rights to information and self-determination in diagnostic genetic testing upheld? A comparison of patients' and providers' perceptionsTarja Nyrhinen, Marja Hietala, Pauli Puukka, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 4, 2020
Wilson's Disease in Finland: A Nationwide Population-Based StudyJussi O T Sipilä, Marja Hietala, Ville Kytö, et al.
Neurology. Genetics|May 16, 2019
HTT haplogroups in Finnish patients with Huntington diseaseSusanna Ylönen, Jussi O T Sipilä, Marja Hietala, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalitiesMaila Penttinen, Hannele Koillinen, Harri Niinikoski, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Duodecim; Laaketieteellinen Aikakauskirja|August 7, 2015
[Parkinson's disease associated with a mutation in the PARK2 gene]Valtteri Kaasinen, Marja Hietala, Mikko Kuoppamäki
New Genetics and Society|October 9, 2004
Ethical issues in the diagnostic genetic testing processTarja Nyrhinen, Helena Leino-Kilpi, Marja Hietala
Clinical and Translational Allergy|June 27, 2017
Food allergy in a child with de novo <i>KAT6A</i> mutationVarpu Elenius, Tuire Lähdesmäki, Marja Hietala, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
A 69-year-old woman with Coffin-Siris syndromeLaura Määttänen, Marja Hietala, Jaakko Ignatius, et al.
Nursing Ethics|April 27, 2007
Privacy and equality in diagnostic genetic testingTarja Nyrhinen, Marja Hietala, Pauli Puukka, et al.
Neurology. Genetics|April 12, 2016
Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutationMika H Martikainen, Markku Päivärinta, Marja Hietala, et al.
Journal of Genetic Counseling|November 4, 2008
Are patient rights to information and self-determination in diagnostic genetic testing upheld? A comparison of patients' and providers' perceptionsTarja Nyrhinen, Marja Hietala, Pauli Puukka, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 4, 2020
Wilson's Disease in Finland: A Nationwide Population-Based StudyJussi O T Sipilä, Marja Hietala, Ville Kytö, et al.
Neurology. Genetics|May 16, 2019
HTT haplogroups in Finnish patients with Huntington diseaseSusanna Ylönen, Jussi O T Sipilä, Marja Hietala, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalitiesMaila Penttinen, Hannele Koillinen, Harri Niinikoski, et al.
Pageof 4