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Sorri, Martti
55  results:
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1

New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:

Skarp, Sini ; Korvala, Johanna ; Kotimäki, Jouko...
Genes.  13 (2022)  6 - p. 998 , 2022
Link: https://doi.org/10.3390/..
 
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2

New genetic variants in CYP2B6 and SLC6A support the role o..:

Skarp, S. (Sini) ; Korvala, J. (Johanna) ; Kotimäki, J. (Jouko)... , 2022
Link: http://urn.fi/urn:nbn:fi..
 
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3

New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:

Sini Skarp ; Johanna Korvala ; Jouko Kotimäki...
Human Genomics and Genetic Diseases.  , 2022
Link: https://doi.org/10.3390/..
 
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4

New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:

Sini Skarp ; Johanna Korvala ; Jouko Kotimäki...
https://www.mdpi.com/2073-4425/13/6/998.  , 2022
Link: https://doi.org/10.3390/..
 
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5

New Genetic Variants in CYP2B6 and SLC6A Support the Role o..:

Skarp, Sini ; Korvala, Johanna ; Kotimäki, Jouko...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222295/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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6

The impact of cardiovascular diseases on hearing deteriorat..:

Venla Lohi (11667977) ; Pasi Ohtonen (23982) ; Martti Sorri (4438531)..
https://figshare.com/articles/journal_contribution/The_impact_of_cardiovascular_diseases_on_hearing_deterioration_a_13-year_follow-up_study/16964711.  , 2021
Link: https://doi.org/10.6084/..
 
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7

The impact of cardiovascular diseases on hearing deteriorat..:

Lohi, V. (Venla) ; Ohtonen, P. (Pasi) ; Sorri, M. (Martti).. , 2021
Link: http://urn.fi/urn:nbn:fi..
 
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8

Prevalence and incidence of hearing impairment among adults..:

Lohi, V. (Venla) ; Ohtonen, P. (Pasi) ; Sorri, M. (Martti).. , 2021
Link: http://urn.fi/urn:nbn:fi..
 
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9

Whole‐exome sequencing suggests multiallelic inheritance fo..:

Skarp, Sini ; Kanervo, Laura ; Kotimäki, Jouko...
Annals of Human Genetics.  83 (2019)  6 - p. 389-396 , 2019
Link: https://doi.org/10.1111/..
 
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10

Hearing impairment is common among Saami adults in Northern..:

Lohi, Venla ; Ohtonen, Pasi ; Aikio, Pekka...
International Journal of Circumpolar Health.  76 (2017)  1 - p. 1398004 , 2017
Link: https://doi.org/10.1080/..
 
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11

A nonsynonymous mutation in the WFS1 gene in a Finnish fami..:

Kytövuori, Laura ; Hannula, Samuli ; Mäki-Torkko, Elina..
Hearing Research.  355 (2017)  - p. 97-101 , 2017
Link: https://doi.org/10.1016/..
 
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12

Hearing impairment is common among Saami adults in Northern..:

Venla Lohi ; Pasi Ohtonen ; Pekka Aikio...
http://dx.doi.org/10.1080/22423982.2017.1398004.  , 2017
Link: https://doi.org/10.1080/..
 
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13

Mutations in the two ribosomal RNA genes in mitochondrial D..:

Häkli, Sanna ; Luotonen, Mirja ; Sorri, Martti.
BMC Medical Genetics.  16 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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14

Kysynnän jousto - Suomeen soveltuvat käytännön ratkaisut ja..:

Järventausta, Pertti ; Repo, Sami ; Trygg, Petri...
978-952-15-3486-7.  , 2015
Link: https://trepo.tuni.fi/ha..
 
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15

Kysynnän jousto - Suomeen soveltuvat käytännön ratkaisut ja..:

Järventausta, Pertti ; Repo, Sami ; Trygg, Petri...
978-952-15-3485-0.  , 2015
Link: https://trepo.tuni.fi/ha..
 
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