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European Journal of Neurology
|
January 24, 2023
Long-term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophy
Victoria 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-Sequencing
Swethaa 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 spectrum
Maria 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 cohort
Victoria Lillback, Gaber Bergant, Maria Francesca Di Feo, et al.
Genome Medicine
|
February 26, 2026
A comprehensive framework for the interpretation of TTN missense variants
Maria Francesca Di Feo, Martin Rees, Victoria Lillback, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
European Journal of Neurology
|
January 24, 2023
Long-term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophy
Victoria 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-Sequencing
Swethaa 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 spectrum
Maria 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 cohort
Victoria Lillback, Gaber Bergant, Maria Francesca Di Feo, et al.
Genome Medicine
|
February 26, 2026
A comprehensive framework for the interpretation of TTN missense variants
Maria Francesca Di Feo, Martin Rees, Victoria Lillback, et al.
Page
of 1