DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter

Observation of ϒ(1S)+Z Associated Production and Measurement of the Effective Double-Parton Scattering Cross Section in Proton-Proton Collisions at sqrt[s]=13 TeV.

Physical review letters·2026

Observation of Nuclear Suppression in Coherent ϒ(1S) Photoproduction off Heavy Nuclei at the LHC.

Physical review letters·2026

Search for Electroweakinos in Compressed-Spectrum Scenarios with Low-Momentum Isolated Tracks in Proton-Proton Collisions at sqrt[s]=13 TeV.

Physical review letters·2026

Combination of ATLAS and CMS Searches for Higgs Boson Pair Production at sqrt[s]=13 TeV.

Physical review letters·2026

Search for the Nonresonant Production of a Pair of Additional Higgs Bosons in the Type-X Two-Higgs-Doublet Model in Proton-Proton Collisions at sqrt[s]=13 TeV.

Physical review letters·2026

Search for Associated Production of a Higgs Boson and Two Vector Bosons via Vector-Boson Scattering at sqrt[s]=13 TeV.

Physical review letters·2026

Uterine leiomyomas in HLRCC: a scoping review of presentation, histopathology, treatment patterns, and reproductive implications.

European journal of human genetics : EJHG·2026

Maternal perspectives on sharing newborn genomic data.

European journal of human genetics : EJHG·2026

RNA sequencing significantly improves HYDIN diagnosis and defines the effects of common deletions in primary ciliary dyskinesia.

European journal of human genetics : EJHG·2026

Optimized RNA-seq workflow for routine diagnosis of mitochondrial diseases using aberrant expression analysis and phenotype-driven prioritization.

European journal of human genetics : EJHG·2026

Characterisation of a Portuguese origin founder missense variant in MSH6.

European journal of human genetics : EJHG·2026

Genetic testing and counselling of patients with monogenic amyotrophic lateral sclerosis in Northern Finland: a retrospective, single-centre study.

European journal of human genetics : EJHG·2026

Genome-wide characterisation of leaf rust resistance loci in an Eastern European barley collection.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

Next-Generation Sequencing to Identify Genetic Causes of Chinese Patients Affected With Non-retinal Developmental Eye Disorders.

Human mutation·2026

Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs.

Frontiers in genetics·2026

Comprehensive genetic screening of the South African Parkinson's disease study collection using the NeuroBooster array.

Clinical parkinsonism & related disorders·2026

Preimplantation genetic testing for KIT-associated pigmentary monogenic diseases.

Frontiers in medicine·2026

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations.

Journal of clinical laboratory analysis·2026

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DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter

Related Concept Videos

Observation of ϒ(1S)+Z Associated Production and Measurement of the Effective Double-Parton Scattering Cross Section in Proton-Proton Collisions at sqrt[s]=13 TeV.

Observation of Nuclear Suppression in Coherent ϒ(1S) Photoproduction off Heavy Nuclei at the LHC.

Search for Electroweakinos in Compressed-Spectrum Scenarios with Low-Momentum Isolated Tracks in Proton-Proton Collisions at sqrt[s]=13 TeV.

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Uterine leiomyomas in HLRCC: a scoping review of presentation, histopathology, treatment patterns, and reproductive implications.

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RNA sequencing significantly improves HYDIN diagnosis and defines the effects of common deletions in primary ciliary dyskinesia.

Optimized RNA-seq workflow for routine diagnosis of mitochondrial diseases using aberrant expression analysis and phenotype-driven prioritization.

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Genetic testing and counselling of patients with monogenic amyotrophic lateral sclerosis in Northern Finland: a retrospective, single-centre study.

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Next-Generation Sequencing to Identify Genetic Causes of Chinese Patients Affected With Non-retinal Developmental Eye Disorders.

Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs.

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Preimplantation genetic testing for KIT-associated pigmentary monogenic diseases.

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations.

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DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter

Abstract:

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