• A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioning
• A Case of WAGR Syndrome with Peters' Anomaly
• A case with WAGR syndrome diagnosed and treated by multidisciplinary combination
• A CGH array procedure to detect PAX6 gene structural defects
• A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome
• A nonsense <em>PAX6</em> mutation in a family with congenital aniridia
• A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor
• A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region
• An uncommon presentation of WAGR syndrome with persistent fetal vasculature
• An X-linked agammaglobulinemia contiguous gene syndrome with metachronous coprimary testicular cancers
• Aniridia
• Aniridia
• Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care ("aniridia guide")
• Aniridic Fibrosis Syndrome
• Aniridic Fibrosis Syndrome
• Array CGH analysis of a cohort of Russian patients with intellectual disability
• Bilateral aniridia and congenital ureteral valve: Role of genetic testing
• Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins
• Bitot-like spots in children with normal vitamin A levels
• Central Corneal Pyogenic Granuloma in Aniridia
• Characteristics of Nephroblastoma/Nephroblastomatosis in Children with a Clinically Reported Underlying Malformation or Cancer Predisposition Syndrome
• Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review
• Clinical Aspects of WT1 and the Kidney
• Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience
• Common genetic and epigenetic syndromes
• Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome
• Congenital aniridia in children
• Congenital Aniridia with Ectopia Lentis
• Correction: The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
• Correlation of Cerebrospinal Fluid Total Protein and Serum Neutrophil-to-Lymphocyte Ratio with Clinical Outcomes of Guillain-Barre Syndrome Variants
• Denys-Drash syndrome associated WT1 glutamine 369 mutants have altered sequence-preferences and altered responses to epigenetic modifications
• Dysgerminoma developing from an ectopic ovary in a patient with WAGR syndrome: A case report
• Endogenous melatonin and sleep in individuals with Rare Genetic Neurodevelopmental Disorders (RGND): A systematic review
• Epidemiology of <em>PAX6</em> Gene Pathogenic Variants and Expected Prevalence of <em>PAX6</em>-Associated Congenital Aniridia across the Russian Federation: A Nationwide Study
• Facial dysostoses: Etiology, pathogenesis and management
• Genetics and epidemiology of aniridia: Updated guidelines for genetic study
• Genetics and epidemiology of aniridia: Updated guidelines for genetic study
• Genetics of congenital aniridia
• Haploinsufficiency of the brain-derived neurotrophic factor gene is associated with reduced pain sensitivity
• Heterogeneity of human WT1 gene
• Identification of a 6-month-old baby with a combination of WAGR and Potocki-Shaffer contiguous deletion syndromes by SNP array testing
• Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH
• Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal Hypoplasia
• LGR4/GPR48 inactivation leads to aniridia-genitourinary anomalies-mental retardation syndrome defects
• LMO2 gene deletions significantly worsen the prognosis of Wilms' tumor development in patients with WAGR syndrome
• Long-term outcome in pediatric renal tumor survivors: experience of a single center
• Malformation syndromes associated with disorders of sex development
• Malformations, genetic abnormalities, and Wilms tumor
• Management of Bilateral Wilms Tumours
• Management of bilateral Wilms tumours
• Management of bilateral Wilms tumours
• Many faces of Wilms Tumor: Recent advances and future directions
• Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations
• Multiple Perianal Epidermal Cysts Found in a Case of Lowe Syndrome: A Case Report and Review of the Literature
• Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4
• National protocol for diagnosis and care of congenital aniridia: Summary for the attending physician
• Nephron-sparing Surgery for Syndromic Wilms' Tumor: Robotic Approach
• Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder
• NGF and BDNF in pediatrics syndromes
• Novel Intragenic <em>PAX6</em> Deletion in a Pedigree with Aniridia, Morbid Obesity, and Diabetes
• Obesity in Childhood and Adolescence, Genetic Factors
• Oculocerebrorenal syndrome of Lowe protein controls cytoskeletal reorganisation during human platelet spreading
• Pediatric Delayed Union in the Presence of WAGR Syndrome
• Potocki-Shaffer syndrome revealed in a WAGR syndrome case with multiple exostoses
• Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome
• Prenatal Diagnosis of WAGR Syndrome
• Rare Syndromes and Common Variants of the Brain-Derived Neurotrophic Factor Gene in Human Obesity
• Renal involvement in tuberous sclerosis complex with emphasis on cystic lesions
• Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management
• Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group
• Risk factors for post-nephrectomy hypotension in pediatric patients
• Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations
• Sequences of COVID-19 in a child with WAGR syndrome: A case report
• Successful Management of Velopharyngeal Insufficiency in WAGR syndrome with Deletion of Chromosome 11p14.3
• Successful stem cell transplantation in a child with chronic granulomatous disease associated with contiguous gene deletion syndrome and complicated by macrophage activation syndrome
• Sustained endocrine profiles of a girl with WAGR syndrome
• Syndromic Wilms tumor: a review of predisposing conditions, surveillance and treatment
• The Directions Are on the Box
• The genetic architecture of aniridia and Gillespie syndrome
• The Largest Germline Heterozygous Deletion Encompassing Potocki-Shaffer and WAGR Syndromes Loci to Date: A Case Report
• The oculocerebrorenal syndrome of Lowe: an update
• The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene
• Thirty Years' History since the Discovery of Pax6: From Central Nervous System Development to Neurodevelopmental Disorders
• Transconjunctival XEN45 implantation for secondary open-angle glaucoma management in a pediatric patient with WAGR syndrome
• Tumor predisposition syndromes and nephroblastoma : Early diagnosis with imaging
• Typical WAGR syndrome in a case
• Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases
• Visual Acuity in Aniridia and WAGR Syndrome
• WAGR syndrome
• WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion
• WAGR syndrome by heterozygous deletion of the WT1 gene. Pediatric case report
• WAGR, Sex Reversal, Bilateral Gonadoblastomas, and Intralobar Nephrogenic Rests: Uncertainties of Pre-Biopsy Chemotherapy in a High Risk Syndrome for Nephroblastoma
• WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities
• Wilms tumor characteristics, surgical management, outcomes, and chronic kidney disease in children with WAGR syndrome: A report from the International WAGR Syndrome Association survey
• Wilms Tumor Gene 1: Lessons from Kidney Development and Cancer
• Wilms tumor in horseshoe kidney in case of WAGR syndrome with multiple congenital anomalies: A cytologic diagnosis
• Wilms tumor: an update
• Wilms' tumor gene 1: lessons from the interface between kidney development and cancer
• WT1 microdeletion and slowly progressing focal glomerulosclerosis in a patient with male pseudohermaphroditism, childhood leukemia, Wilms tumor and cerebellar angioblastoma
• WT1-related disorders: more than Denys-Drash syndrome