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Publications by Vytautas Ivaškevičius
Characterization of a Novel Large Deletion Caused by Double-Stranded Breaks in 6-Bp Microhomologous Sequences of Intron 11 and 12 of the F13A1 Gene
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Related publications
Further Delineation of the Phenotype Caused by a Novel Large Homozygous Deletion of GRID2 Gene in an Adult Patient
Clinical Case Reports
Medicine
Phenotype and Genotype of FXIII Deficiency in Two Unrelated Probands: Identification of a Novel F13A1 Large Deletion Mediated by Complex Rearrangement
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Identification and Characterization of a Novel 43-Bp Deletion Mutation of the ATP7B Gene in a Chinese Patient With Wilson’s Disease: A Case Report
BMC Medical Genetics
Genetics
Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Figure 6: Alignment of murC Gene Sequences in UM_3 (396bp) and UM_11 (495 Bp).
Double-Stranded RNA Bending by AU-tract Sequences
Apparent Homozygosity of p.Phe508del inCFTRdue to a Large Gene Deletion of Exons 4–11
Case Reports in Genetics
A Novel Double Deletion Underscores the Importance of Characterizing End Points of the CFTR Large Rearrangements
European Journal of Human Genetics
Genetics
Deletion of Alu Sequences in the Fifth C-Sis Intron in Individuals With Meningiomas.
Journal of Clinical Investigation
Medicine
