Gezielt nachschlagen
Suche
Suche startet nach einer kurzen Eingabepause.
Seite 6 für „Genetic“ · Literaturverweise aus öffentlichen Artikeln
Suchtreffer
Quellen in Artikeln
Genetic architecture of lumbar spinal stenosis
pubmed · 41942452
Literaturverweis öffnenUncovering the cytogenetic hallmarks of resident and expanded natural killer cells from patients with acquired aplastic anemia
pubmed · 42448949
Literaturverweis öffnen[Asthma as a chronic desquamative eosinophilic bronchitis. Studies on the pathogenetic significance of hypodense eosinophilic granulocytes in bronchial asthma].
pubmed · 1924196
Literaturverweis öffnenThe Complex Clinical and Genetic Landscape of Hereditary Peripheral Neuropathy
pubmed · 33497257
Literaturverweis öffnenGenetic and environmental contributions to dental fluorosis in the primary dentition: A census-based twin study
pubmed · 42029364
Literaturverweis öffnen[Familial tooth position anomalies in the Orangutang. Orthodontic, cytogenetic and anthropological studies].
pubmed · 6576969
Literaturverweis öffnenAndrogenetic alopecia risk in allergic rhinitis: A cohort study of immune and antihistamine effects
pubmed · 42028243
Literaturverweis öffnenGenetic analysis of TGFBI variants in the Taiwanese population: from granular corneal dystrophy type 1 to a broader phenotypic spectrum
pubmed · 42325762
Literaturverweis öffnenCorrelation of UGT1A1 genotypes with newborn hyperbilirubinemia using newborn genetic screening
pubmed · 42483412
Literaturverweis öffnenInteraction between dietary cholesterol intake and genetic variants for cholesterol absorption in relation to coronary artery disease mortality: a prospective analysis in the Singapore Chinese Health Study
pubmed · 40935150
Literaturverweis öffnenGenetic analysis of the SRD5A2 gene in Indian patients with 5alpha-reductase deficiency
pubmed · 19492581
Literaturverweis öffnenCorrelation between tricuspid regurgitation and fetal cardiac structure or signs and prenatal genetic testing abnormalities in fetuses at 12+ 0 to 16+ 0 weeks of gestation
pubmed · 42210096
Literaturverweis öffnenBlood-based RBBP7 and RIBC1 methylation as a candidate epigenetic biomarker for ovarian cancer epigenetic markers RBBP7 and RIBC1 in ovarian cancer.
pubmed · 42525292
Literaturverweis öffnenInherited epidermolysis bullosa: update on the clinical and genetic aspects
pubmed · 32732072
Literaturverweis öffnenGenetic Analysis of Isolated Hepatic Ductal Plate Malformation Reveals Novel Variants and Insights into Phenotypic Correlation
pubmed · 42365546
Literaturverweis öffnenAcrokeratosis verruciformis of Hopf: Genetic, clinicopathologic and therapeutic features (Review)
pubmed · 42205461
Literaturverweis öffnenPrevalence and Genetic Spectrum of Inherited Kidney Diseases: A Chinese Cohort Study
pubmed · 41920701
Literaturverweis öffnenSertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms
pubmed · 36814036
Literaturverweis öffnenGenotype-phenotype correlation in alpha-thalassemia: predicting genetic subgroups via laboratory parameters
pubmed · 42239965
Literaturverweis öffnenGenetic and Environmental Contributions to Antisocial Personality Disorder
doi · 10.20944/preprints202601.2358.v1
Literaturverweis öffnenFamilial lymphoma and genetic predisposition: an updated review
pubmed · 42316213
Literaturverweis öffnen[Legasthenia from the genetic viewpoint].
pubmed · 6358770
Literaturverweis öffnenCurrarino syndrome: a comprehensive genetic review of a rare congenital disorder
pubmed · 33836786
Literaturverweis öffnen[Cat-scratch disease: historical, clinical, phylogenetic and taxonomic aspects].
pubmed · 9198973
Literaturverweis öffnenExome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia: An International Consortium Study
pubmed · 39700446
Literaturverweis öffnenA finding in genetic polymorphism analysis study: A case of non-mosaic 47, XXX without manifestations
pubmed · 28697408
Literaturverweis öffnenClinical impact of genetic testing in inherited kidney diseases
pubmed · 42389199
Literaturverweis öffnenPoints to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG)
pubmed · 41615347
Literaturverweis öffnenHuman Genetics of Ventricular Septal Defect
pubmed · 38884729
Literaturverweis öffnen