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20 results on '"Sablauskas, Karolis"'

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1. Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

2. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

4. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

5. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

6. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

7. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

8. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

10. A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

11. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

14. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

15. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

16. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

17. Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)

18. Heterogenous Serological Responses to BNT162b2 mRNA Vaccine in Patients with Haematological Malignancies

20. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

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