Associated Papers
Genomic characterization of lymphomas in patients with inborn errors of immunity.
Ye X et al.
Blood Advances, 2022
35687490 (PubMed )
Supplement: advancesADV2021006654-suppl4.xlsx › PL21__PON_in_red_
Searching for the Molecular Basis of Partial Deafness.
Oziębło D et al.
International Journal of Molecular Sciences, 2022
35682719 (PubMed )
Supplement: ijms-23-06029-s001.zip › TableS2.xlsx › Arkusz
Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease.
Escalera-Balsera A et al.
Genes, 2020
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.
Roman-Naranjo P et al.
Ear and Hearing, 0
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