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Victoria Lillback

Showing results (1-10 of 5) with videos related to

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European Journal of Neurology|January 24, 2023
Long-term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophyVictoria Lillback, Marco Savarese, Niina Sandholm, et al.
BMC Genomics|May 14, 2026
Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-SequencingSwethaa Natraj Gayathri, Victoria Lillback, Bjarne Udd, et al.
Journal of Medical Genetics|March 28, 2023
The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrumMaria Francesca Di Feo, Victoria Lillback, Manu Jokela, et al.
Journal of Medical Genetics|March 5, 2025
Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohortVictoria Lillback, Gaber Bergant, Maria Francesca Di Feo, et al.
Genome Medicine|February 26, 2026
A comprehensive framework for the interpretation of TTN missense variantsMaria Francesca Di Feo, Martin Rees, Victoria Lillback, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
European Journal of Neurology|January 24, 2023
Long-term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophyVictoria Lillback, Marco Savarese, Niina Sandholm, et al.
BMC Genomics|May 14, 2026
Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-SequencingSwethaa Natraj Gayathri, Victoria Lillback, Bjarne Udd, et al.
Journal of Medical Genetics|March 28, 2023
The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrumMaria Francesca Di Feo, Victoria Lillback, Manu Jokela, et al.
Journal of Medical Genetics|March 5, 2025
Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohortVictoria Lillback, Gaber Bergant, Maria Francesca Di Feo, et al.
Genome Medicine|February 26, 2026
A comprehensive framework for the interpretation of TTN missense variantsMaria Francesca Di Feo, Martin Rees, Victoria Lillback, et al.
Pageof 1