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Seite 5 für „Genetic“ · Literaturverweise aus öffentlichen Artikeln
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EndoGene database: reported genetic variants for 5,926 Russian patients diagnosed with endocrine disorders
pubmed · 40041282
Literaturverweis öffnenRadiogenomics of congenital brain malformations: Linking embryology, genetics, and imaging
pubmed · 41670708
Literaturverweis öffnen[Androgenetic alopecia: finasteride treated hair loss].
pubmed · 10230220
Literaturverweis öffnenClinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon
pubmed · 42230379
Literaturverweis öffnenIdentifying common genetic etiologies between iridocyclitis and related immune-mediated diseases
pubmed · 41624885
Literaturverweis öffnenCerebral palsy: causes, pathways, and the role of genetic variants
pubmed · 26003063
Literaturverweis öffnenThe distinct effects of metabolic syndrome on negative symptoms and on antipsychotic therapy of schizophrenia involve insular volume, functional connectivity, and genetic polymorphisms
pubmed · 42386701
Literaturverweis öffnenGenetics of Hb F/F Cell Variance in Adults and Heterocellular Hereditary Persistence of Fetal Hemoglobin
pubmed · 9859924
Literaturverweis öffnen[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]
pubmed · 36241230
Literaturverweis öffnenCorrection to: Gastrointestinal juvenile-like (inflammatory/hyperplastic) mucosal polyps in neurofibromatosis type 1 with no concurrent genetic or clinical evidence of other syndromes
pubmed · 30306267
Literaturverweis öffnenHas the introduction of increased genetic prenatal testing affected rates of termination of pregnancy due to fetal abnormality?
pubmed · 38348952
Literaturverweis öffnenA novel ensemble-based genetic algorithm for enhanced feature selection in lung and pancreatic cancer diagnosis
pubmed · 42237052
Literaturverweis öffnen<scp>Schimmelpenning–Feuerstein–Mims</scp> syndrome: A case series and brief literature review of genetically ascertained cases
pubmed · 36377817
Literaturverweis öffnenIntegrating clinical and genetic insights in anterior segment dysgenesis with glaucoma: A contemporary review
pubmed · 41936534
Literaturverweis öffnenAPPROACH TO THE PATIENT: Genetics and Management of Congenital Hypothyroidism
pubmed · 42170892
Literaturverweis öffnenCorrection to 'Programmed Cell Death 1 Genetic Variant and Liver Damage in Nonalcoholic Fatty Liver Disease'
pubmed · 42387839
Literaturverweis öffnenErratum for the Research Article "ATP citrate lyase drives vascular remodeling in systemic and pulmonary vascular diseases through metabolic and epigenetic changes"
pubmed · 41849584
Literaturverweis öffnenA Signaling-Threshold Framework for Human Tooth Agenesis: Integrating Molecular Genetics with Developmental Field Theory
pubmed · 42196506
Literaturverweis öffnenClinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines
pubmed · 42433928
Literaturverweis öffnenA Clinician's Guide to Celiac Disease HLA Genetics
pubmed · 31274511
Literaturverweis öffnenThe Multifactorial Causes of Down Syndrome During Pregnancy: A Narrative Review of Genetic, Environmental, and Maternal Influences
pubmed · 41356612
Literaturverweis öffnenAn atlas of genetic determinants of forearm fracture
pubmed · 37919453
Literaturverweis öffnenEpidemiology, Genetic Recombination, and Pathogenesis of Coronaviruses
pubmed · 27012512
Literaturverweis öffnen[Immunogenetic studies in patients with IgM rheumatoid factor negative erosive chronic polyarthritis (c.p.)].
pubmed · 3460283
Literaturverweis öffnenHair growth stimulated by allogenic adipose-derived stem cells supplemented with ATP in a mouse model of dihydrotestosterone-induced androgenetic alopecia
pubmed · 40483511
Literaturverweis öffnenCase Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype
pubmed · 41816679
Literaturverweis öffnenVisual outcomes of scleral-fixated posterior chamber intraocular lenses in children with genetic ectopia lentis: long-term follow-up
pubmed · 42260393
Literaturverweis öffnen[Genetic analysis of one family with congenital limb malformations]
pubmed · 31515783
Literaturverweis öffnenImmunohistochemical and genetic characteristics of HPV-associated endocervical carcinoma with an invasive stratified mucin-producing carcinoma (ISMC) component
pubmed · 34103667
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