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Seite 3 für „Genetic“ · Literaturverweise aus öffentlichen Artikeln
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"Familial Is Not Always Genetic: Two Brothers with Dystonia and Oculomotor Apraxia Secondary to Rh Incompatibility-Induced Kernicterus"
pubmed · 42340156
Literaturverweis öffnenCorrigendum: Deepening insights into cholinergic agents for intraocular pressure reduction: systems genetics, molecular modeling, and in vivo perspectives
pubmed · 39430956
Literaturverweis öffnenThe Genetics of Familial Neoplastic Thyroid Disease and Primary Hyperparathyroidism
pubmed · 42419309
Literaturverweis öffnen‘The psychosocial burden of alopecia areata and androgenetica’: a cross‐sectional multicentre study among dermatological out‐patients in 13 European countries
pubmed · 31465592
Literaturverweis öffnenUnraveling the Clinical and Genetic Landscape of Talipes Equinovarus (Clubfoot)
pubmed · 41884749
Literaturverweis öffnenImpaired Myogenic Differentiation Is a Shared Feature Across Genetic Myopathies
pubmed · 42511681
Literaturverweis öffnenExploring the Genetic Association and Genetic Architecture of Iridocyclitis and Extraocular Autoimmune Diseases
pubmed · 41677390
Literaturverweis öffnenNeonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes?
pubmed · 34733806
Literaturverweis öffnenGenetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications
pubmed · 38699388
Literaturverweis öffnenOculocutaneous albinism: epidemiology, genetics, skin manifestation, and psychosocial issues
pubmed · 35217926
Literaturverweis öffnenA genome-wide association study of problematic sexual behaviour: genetic overlap with psychiatric, behavioural and personality phenotypes
doi · 10.64898/2026.05.15.26351052
Literaturverweis öffnenVascular Mechanisms in the Etiology of Hemifacial Microsomia: A Systematic Review of Epidemiological, Clinical, and Genetic Evidence
pubmed · 42322171
Literaturverweis öffnenNext-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic Heterogeneity
pubmed · 32036089
Literaturverweis öffnenMolecular and genetic analysis of iron uptake proteins in the Brazilian purpuric fever clone of Haemophilus influenzae biogroup aegyptius
pubmed · 9727086
Literaturverweis öffnenSurgical View of Morphological and Pathogenetic Identity of Pilonidal Cysts and Acne Inversa
pubmed · 36047363
Literaturverweis öffnenRadiation therapy, cytogenetic prognostication, novel systemic chemotherapy, and patient perspective in an adult with choroidal melanoma
pubmed · 42267753
Literaturverweis öffnenHuman Genetics of Truncus Arteriosus
pubmed · 38884753
Literaturverweis öffnenGenetic Skeletal Disorders with Defects in Glycosaminoglycan Biosynthesis
pubmed · 42094029
Literaturverweis öffnenDissecting the Genetic Architecture of Tanning and Sunburn as Skin Cancer Risk Factors
pubmed · 41167550
Literaturverweis öffnenGenetics of CAKUT
pubmed · 41710414
Literaturverweis öffnenGenetic Hearing Loss Overview
pubmed · 20301607
Literaturverweis öffnenGenetic diagnosis of macrotia in PIK3CA-Related Overgrowth Spectrum (PROS) and long-term outcome of otoplasty: a case report and literature review
pubmed · 41650668
Literaturverweis öffnen[Genetic, endocrine, drug-induced and pancreatogenic forms of diabetes and exocrine pancreatic insufficiency (Update 2026)]
pubmed · 42162477
Literaturverweis öffnenGenetics, Cytogenetic Testing and Conventional Karyotype
pubmed · 33085440
Literaturverweis öffnenKidney outcomes of coenzyme Q10 supplementation in patients with genetically confirmed CoQ10 nephropathy in Japan
pubmed · 42435122
Literaturverweis öffnenJoint contributions of genetic risk and pubertal maturation to internalizing symptoms in adolescents
doi · 10.31234/osf.io/5fw8q_v1
Literaturverweis öffnenCurrarino syndrome: a comprehensive genetic review of a rare congenital disorder
pubmed · 33836786
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