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Paakkola, Teija
8  Ergebnisse:
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1

Comparison of the ABC and ACMG systems for variant classifi..:

Houge, Gunnar ; Bratland, Eirik ; Aukrust, Ingvild...
European Journal of Human Genetics.  32 (2024)  7 - p. 858-863 , 2024
Link: https://doi.org/10.1038/..
 
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2

Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic an..:

Keskinen, Sini ; Paakkola, Teija ; Mattila, Mirjami...
Pediatric and Developmental Pathology.  27 (2023)  2 - p. 181-186 , 2023
Link: https://doi.org/10.1177/..
 
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3

Biallelic mutations in human NHLRC2 enhance myofibroblast d..:

Paakkola, Teija ; Salokas, Kari ; Miinalainen, Ilkka...
Human Molecular Genetics.  , 2018
Link: https://doi.org/10.1093/..
 
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4

NHLRC2 variants identified in patients with fibrosis, neuro..:

Uusimaa, Johanna ; Kaarteenaho, Riitta ; Paakkola, Teija...
Acta Neuropathologica.  135 (2018)  5 - p. 727-742 , 2018
Link: https://doi.org/10.1007/..
 
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5

NHLRC2 variants identified in patients with fibrosis, neuro..:

Uusimaa, Johanna ; Kaarteenaho, Riitta ; Paakkola, Teija...
10.1007/s00401-018-1817-z.  , 2019
Link: http://hdl.handle.net/10..
 
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6

NHLRC2 variants identified in patients with fibrosis, neuro..:

Uusimaa, Johanna ; Kaarteenaho, Riitta ; Paakkola, Teija.
1432-0533.  , 2018
Link: https://trepo.tuni.fi/ha..
 
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7

sj-docx-1-pdp-10.1177_10935266231210155 – Supplemental mate..:

Sini Keskinen ; Teija Paakkola ; Mirjami Mattila...
doi:10.25384/sage.24591851.v1.  , 2023
Link: https://doi.org/10.25384..
 
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8

Novel genetic causes and functional studies of severe neuro..:

Paakkola, T. (Teija) , 2019
Link: http://urn.fi/urn:isbn:9..
 
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