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Seite 20 für „Gene“ · Literaturverweise aus öffentlichen Artikeln
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Underrecognized triploidy and genome-wide uniparental disomy in human blastocysts revealed by a concurrent preimplantation genetic testing approach
pubmed · 42293311
Literaturverweis öffnenChromobox 3 assembles an epigenetic complex contributing to cystathionine γ-lyase-mediated protection against aortic aneurysm/dissection
pubmed · 42236713
Literaturverweis öffnenUrinary Diversion with Left Sided Ileal Conduit for Neurogenic Bladder in a Patient with Sacral Agenesis and Situs Inversus: A Case Report
pubmed · 41782987
Literaturverweis öffnenCARD14-Associated Papulosquamous Eruption (CAPE): An Updated Review of Pathogenesis and Treatment
pubmed · 41845528
Literaturverweis öffnenPatterns of Mandibular Incisor Agenesis in Japanese Patients With Non-syndromic Oligodontia: A Retrospective Study
pubmed · 41737120
Literaturverweis öffnenCorrigendum: IgG2 rules: N-acetyl-β-D-glucosamine-specific IgG2 and Th17/Th1 cooperation may promote the pathogenesis of acute rheumatic heart disease and be a biomarker of the autoimmune sequelae of Streptococcus pyogenes
pubmed · 37719980
Literaturverweis öffnen[X-chromosomal recessive ichthyosis. Detection of heterozygote status in genetically possible carriers by determination of arylsulfatase C activity].
pubmed · 3470217
Literaturverweis öffnenC-Brachydaktylie in vier Generationen
pubmed · 6694344
Literaturverweis öffnenOsteogenesis Imperfecta
pubmed · 1580589
Literaturverweis öffnenFrequency and Prognostic Significance of Genetic Abnormalities in a Subgroup of Patients With Intermediate-Risk Neuroblastoma: A SIOPEN Study
pubmed · 42385103
Literaturverweis öffnenEfficacy of an Anti-Inflammatory Dietary Pattern on Global Functioning, Gut Microbiome, and Health in Patients with Psychiatric Disorders and Neurodegenerative Diseases: Protocol for a Randomized Controlled Crossover Trial
doi · 10.64898/2026.06.02.26354674
Literaturverweis öffnenEvidence-based classification of genes implicated in skeletal disorders using the ClinGen curation framework
pubmed · 41313243
Literaturverweis öffnenBilateral renal and bladder agenesis with exceptional survival without prenatal intervention: a case report
pubmed · 42109486
Literaturverweis öffnenMalignes Mesotheliom der Pleura, des Perikards und des Peritoneums Teil 1: Ätiologie, Pathogenese, Pathologie
pubmed · 11013806
Literaturverweis öffnen[Prenatal cytogenetic diagnosis in a case of craniorachischisis].
pubmed · 4770439
Literaturverweis öffnenA case report and reconsideration of pathogenesis: C5 palsy after corrective surgery for severe congenital cervicothoracic scoliosis
pubmed · 42100013
Literaturverweis öffnenEpidural Stimulation Combined with Triple Gene Therapy for Spinal Cord Injury Treatment
pubmed · 33255323
Literaturverweis öffnenChronic lymphocytic leukemia. Treatment and genetic risk profile
pubmed · 23371259
Literaturverweis öffnenInternal carotid artery agenesis: A narrative review
pubmed · 42232383
Literaturverweis öffnenMicroglia heterogeneity in vascular dementia pathology
pubmed · 42473665
Literaturverweis öffnenPeripheral neuron phenotypes of familial dysautonomia are rescued by AAV-mediated gene therapy
pubmed · 41957238
Literaturverweis öffnenNew insights into the genetics of mandibular retrognathism: novel candidate genes
pubmed · 38296908
Literaturverweis öffnenCardiovascular Disease and Age-Related Macular Degeneration
pubmed · 42134616
Literaturverweis öffnenBiallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology: A Response Letter
pubmed · 42357964
Literaturverweis öffnenGADA testing: preparation for adult general population screening
pubmed · 42118255
Literaturverweis öffnen[Mouth abnormality: to the general practitioner?].
pubmed · 26210537
Literaturverweis öffnenDiabetic impact on the neuroaxis: from peripheral neuropathy to central neurodegeneration
pubmed · 42358680
Literaturverweis öffnenGenetische Diagnostik bei psychischen Erkrankungen im Erwachsenenalter
pubmed · 39316100
Literaturverweis öffnenArrhythmogene rechtsventrikuläre Kardiomyopathie / Dysplasie: Pathogenese, Diagnose und Therapie
pubmed · 28462618
Literaturverweis öffnenSomatisierung - somatoforme Störungen - Ätiopathogenetische Modelle1
pubmed · 11253560
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