Gezielt nachschlagen
Suche
Suche startet nach einer kurzen Eingabepause.
Seite 1 für „phenotype“ · Literaturverweise aus öffentlichen Artikeln
Suchtreffer
Quellen in Artikeln
Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma
pubmed · 28561224
Literaturverweis öffnenPainful gastric glitch: an acute epigastric pain triggered by specific food as a new phenotype of postprandial epigastric pain syndrome
pubmed · 42374305
Literaturverweis öffnenFibrotic phenotype of IgG4-related disease
pubmed · 38574746
Literaturverweis öffnenBlended Phenotype Involving FBN1 and Novel PIGL Variants of Uncertain Significance: A Prenatal Case Report
pubmed · 42377900
Literaturverweis öffnenRisk of Placental Pathology Across Ultrasound-Defined Phenotypes of Impaired Fetal Growth in Dichorionic Twins: A Retrospective Cohort Study
pubmed · 41808584
Literaturverweis öffnenWhen Immunophenotype Is Not Identity: A Clinicopathological Review of Neuroendocrine Differentiation in Tumors of the Female Genital Tract
doi · 10.20944/preprints202605.0193.v1
Literaturverweis öffnenSTAC3D Against the Odds: Characterizing the Musculoskeletal Phenotype of STAC3 Gene Disorder
pubmed · 42490135
Literaturverweis öffnenT cell transfer into immunodeficient mice uncovers a paralytic phenotype beyond colitis
pubmed · 42419956
Literaturverweis öffnenA Novel Digital Phenotype for Burn Sepsis: Leveraging Electronic Health Record Data and Natural Language Processing to Improve Case Definition
pubmed · 42242239
Literaturverweis öffnenRestraint Status Influences Fracture Phenotypes and Operative Management in Pediatric MVC-Related Facial Trauma
pubmed · 42283503
Literaturverweis öffnenGenotype-Phenotype Correlations in Corneal Dystrophies: Advances in Molecular Genetics and Therapeutic Insights
pubmed · 40079222
Literaturverweis öffnenPhenotype-Driven Whole-Exome Sequencing Reanalysis Identifies a Homozygous PPP2R3C Variant in Syndromic 46,XY and 46,XX Gonadal Dysgenesis: Case Report and Review of the Literature
pubmed · 42445464
Literaturverweis öffnenDevelopmental venous anomalies on fetal magnetic resonance imaging: prevalence and reproducible radiological phenotypes
pubmed · 42440099
Literaturverweis öffnenThe fortunate amelioration of Costus speciosus on phenotypes of letrozole-induced polycystic ovary syndrome in female rats
pubmed · 41983838
Literaturverweis öffnenChromosomal abnormalities and pregnancy outcomes in 350 pregnancies with prenatally diagnosed aberrant right subclavian artery: a phenotype-based retrospective cohort study
pubmed · 42219360
Literaturverweis öffnenIdentifying Hemophagocytic Lymphohistiocytosis and Describing Outcomes Using Computable Phenotypes: Retrospective Cohort Study
pubmed · 41886745
Literaturverweis öffnenUsmani-Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant
pubmed · 38665048
Literaturverweis öffnenAssociation between fibrocystic breast disease and polycystic ovarian syndrome phenotypes: A cross-sectional study
pubmed · 41438397
Literaturverweis öffnenPrenatal phenotypes and pregnancy outcomes of fetuses with recurrent 16p13.11 microduplications
pubmed · 42260801
Literaturverweis öffnenLocal Recurrence and Metastasis Define Distinct Recurrence Phenotypes in Soft Tissue Sarcoma
pubmed · 42449644
Literaturverweis öffnenNovel Imaging Phenotype in Spinal Cerebellar Ataxia Type 8: Symmetrical White Matter Changes without Cerebellar Atrophy
pubmed · 42105044
Literaturverweis öffnenA Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype
pubmed · 42160204
Literaturverweis öffnenPsychiatric phenotypes associated with hyperprolinemia: A systematic review
pubmed · 34302426
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 öffnenDoes variation in neurodegenerative disease susceptibility and phenotype reflect cerebral differences at the network level?
pubmed · 23879681
Literaturverweis öffnenDistinct age-dependent phenotypes of abnormal liver function tests derived from national Emergency Department data
pubmed · 42167325
Literaturverweis öffnen