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UnknownNovel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome.
Not available
S-EPMC4589207 | biostudies-literature
UnknownWhole-exome sequencing and its impact in hereditary hearing loss.
Not available
S-EPMC5503681 | biostudies-literature
UnknownT cell immune deficiency rather than chromosome instability predisposes patients with short telomere syndromes to squamous cancers.
Not available
S-EPMC10188244 | biostudies-literature
UnknownAntibody-Conjugated Electrospun Nanofibers for Electrochemical Detection of Methamphetamine.
Not available
S-EPMC10214377 | biostudies-literature
UnknownComprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.
Not available
S-EPMC4641619 | biostudies-literature
UnknownNovel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.
Not available
S-EPMC5679420 | biostudies-literature
UnknownA comparative assessment of clinical efficiency between premium heat-activated copper nickel-titanium and superelastic nickel-titanium archwires during initial orthodontic alignment in adolescents: a randomized clinical trial.
Not available
S-EPMC6911816 | biostudies-literature
UnknownThe Safety of available immunotherapy for the treatment of glioblastoma.
Not available
S-EPMC5404815 | biostudies-literature
UnknownSURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey.
Not available
S-EPMC7586243 | biostudies-literature
UnknownPeptide-Based Regulation of TNF-α-Mediated Cytotoxicity.
Not available
S-EPMC12024540 | biostudies-literature
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