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Seite 7 für „Genetic“ · Literaturverweise aus öffentlichen Artikeln
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Drug-Induced Photosensitivity: Clinical Types of Phototoxicity and Photoallergy and Pathogenetic Mechanisms
pubmed · 36238932
Literaturverweis öffnenTreacher Collins Syndrome: Genetics, Clinical Features and Management
pubmed · 34573374
Literaturverweis öffnenThe Genetics of Familial Neoplastic Thyroid Disease and Primary Hyperparathyroidism
pubmed · 42419309
Literaturverweis öffnenDuplex kidney formation: developmental mechanisms and genetic predisposition
pubmed · 32030122
Literaturverweis öffnenHighlights from JAAD Reviews: Nonpharmacologic and adjunctive treatments for nail psoriasis and androgenetic alopecia
pubmed · 42067036
Literaturverweis öffnenMapping Genetic Susceptibility to Urinary Tract Infection from Kidney Papilla to Bladder
doi · 10.64898/2026.07.07.26357417
Literaturverweis öffnenPrenatal genetic diagnosis and pregnancy outcomes of the surviving co-twin after spontaneous single intrauterine fetal demise
pubmed · 42009805
Literaturverweis öffnenEpigenetics in inflammatory liver diseases: A clinical perspective (Review)
pubmed · 35481220
Literaturverweis öffnenPreimplantation genetic testing and carrier status detection in patients with balanced chromosomal rearrangements: a real-world multicenter retrospective study
pubmed · 40246052
Literaturverweis öffnenCongenital myasthenic syndrome: is it time for a name change to genetic myasthenic syndrome?
pubmed · 41630153
Literaturverweis öffnenHospital-based surveillance suggested a high frequency of congenital rubella syndrome and the presence of genetically diverse genotype 2B rubella virus strains in Ethiopia
pubmed · 42242620
Literaturverweis öffnenClinical and Genetic Landscapes of Mucopolysaccharidosis Type III in 20 Chinese Patients
doi · 10.21203/rs.3.rs-8576442/v1
Literaturverweis öffnen[Portal hypertension and pulmonary hypertension: coincidence or pathogenetic association? Report of two personal cases and review of the literature].
pubmed · 8145680
Literaturverweis öffnenGenetic and functional characterization of inherited complex chromosomal rearrangements in a family with multisystem anomalies
pubmed · 40469905
Literaturverweis öffnenFamilial risks in prostate cancer between brothers and half-brothers as clues to germline genetic and environmental causes
pubmed · 42113346
Literaturverweis öffnenInherited epidermolysis bullosa: update on the clinical and genetic aspects
pubmed · 32732072
Literaturverweis öffnenCurrarino syndrome: a comprehensive genetic review of a rare congenital disorder
pubmed · 33836786
Literaturverweis öffnenImpact of Genetics on Endocrine Manifestations of Cystic Fibrosis
pubmed · 42162871
Literaturverweis öffnenEpidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis
pubmed · 37086676
Literaturverweis öffnenEmerging Genetic Therapy for Sickle Cell Disease
pubmed · 30355263
Literaturverweis öffnenSickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment
pubmed · 33072979
Literaturverweis öffnenGenetic drivers of etiologic heterogeneity in thyroid cancer
pubmed · 42431967
Literaturverweis öffnenGenetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis
pubmed · 30552173
Literaturverweis öffnenCharacteristics, Epigenetics, and Management of Non-Infectious Preterm Birth-Sterile Intrauterine Inflammation and Idiopathic Preterm Birth
pubmed · 42355410
Literaturverweis öffnenFive Pathogenetic Classifications for Alloimmune Hemolytic Disease of the Fetus And Newborn
pubmed · 41520492
Literaturverweis öffnenExpanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani Families
pubmed · 42194996
Literaturverweis öffnenAlpha-Fetoprotein as a Biomarker in Pregnancy: From Genetic Disorders to Obstetric Complications
pubmed · 42193139
Literaturverweis öffnenIKZF1 exacerbates the inflammatory response by epigenetically modulating mitochondrial function following acute peritonitis
pubmed · 41019036
Literaturverweis öffnenCase Report: Two neonatal cases of genetically confirmed junctional epidermolysis bullosa in a tertiary care center
pubmed · 41948702
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