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Seite 2 für „phenotype“ · Literaturverweise aus öffentlichen Artikeln
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49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes
pubmed · 40755837
Literaturverweis öffnenFetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes
pubmed · 33238542
Literaturverweis öffnenAssociation between fibrocystic breast disease and polycystic ovarian syndrome phenotypes: A cross-sectional study
pubmed · 41438397
Literaturverweis öffnenPeripheral neuron phenotypes of familial dysautonomia are rescued by AAV-mediated gene therapy
pubmed · 41957238
Literaturverweis öffnenHematologic Vulnerability in Gestational Hypertension: Platelet-Defined Severity Phenotypes and Maternal Outcomes
pubmed · 42493819
Literaturverweis öffnenGestational homocysteine exposure induces preeclampsia-like phenotypes and alters fetal neurodevelopmental gene expression via impaired decidualization
pubmed · 42409260
Literaturverweis öffnenPrenatal phenotypes and pregnancy outcomes of fetuses with recurrent 16p13.11 microduplications
pubmed · 42260801
Literaturverweis öffnenBeyond "Food Allergy": The Case for Phenotype-Specific Management
pubmed · 42425272
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 öffnenSynchronous Cervical and Vulvar High-Grade Squamous Intraepithelial Lesions with Unusual p16/p53 Immunophenotype: A Case Report
pubmed · 42029466
Literaturverweis öffnenNeurogenic Pelvic Floor Dysfunctions Across Neurological Disorders: Mechanisms, Phenotypes, and Precision Rehabilitation Pathways-A Narrative Review
pubmed · 42452600
Literaturverweis öffnenOphthalmological phenotype associated with biallelic CPAMD8 variants: first report in Mexican patients
pubmed · 41917731
Literaturverweis öffnenNatural senolytic activity of Rhodiola rosea extract alleviates age-associated phenotypes via paraptosis
pubmed · 42028013
Literaturverweis öffnenRHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3
pubmed · 42187878
Literaturverweis öffnenClinical and neuroimaging phenotypes of autoimmune glial fibrillary acidic protein astrocytopathy: A systematic review and meta‐analysis
pubmed · 38506182
Literaturverweis öffnenA highly rare female phenotype with complex chromosomal mosaicism: 46,XY/45,X/46,X,r(Y)
pubmed · 41285118
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 öffnenExpanding the clinical phenotype of HIST1H1E syndrome: cerebellar atrophy and bilateral optic neuropathy, a case report
pubmed · 42318240
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 öffnenCase Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype
pubmed · 41816679
Literaturverweis öffnenUrological Malformations Identify the High-Burden Phenotype Among Children Hospitalized for Presumed Urinary Tract Infection: A Retrospective Cohort
pubmed · 42449890
Literaturverweis öffnenPrimary cutaneous peripheral T-cell lymphomas with a T-follicular helper phenotype: an integrative clinical, pathological and molecular case series study
pubmed · 35895386
Literaturverweis öffnenPrurigo nodularis phenotype in the bullous dermatoses spectrum
pubmed · 40118301
Literaturverweis öffnenSTAC3D Against the Odds: Characterizing the Musculoskeletal Phenotype of STAC3 Gene Disorder
pubmed · 42490135
Literaturverweis öffnenAnti-GPIIIa antibody and CD4 count identify an autoimmune-enriched phenotype of HIV-associated thrombocytopenia: development and internal validation of a clinical nomogram
pubmed · 42483181
Literaturverweis öffnenGenotype-phenotype correlation in alpha-thalassemia: predicting genetic subgroups via laboratory parameters
pubmed · 42239965
Literaturverweis öffnenSrc and β-catenin control a senescence-fibrotic phenotype in uterine fibroid cells
pubmed · 42362678
Literaturverweis öffnenGlucose transporter type 1 deficiency syndrome: Phenotypes, molecular findings, and ketogenic therapy implementation in Argentina
pubmed · 41626780
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