• 25% cluster
• A case of siderosis bulbi without a radiologically detectable foreign body
• A case of unilateral sectoral iris heterochromia in an infant with Beckwith-Wiedemann syndrome
• A Case of Woolly Hair Nevus Associated with Pigmentary Demarcation Lines and Heterochromia Iridis: Coincidence or a New Association?
• A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients
• A comprehensive genotype-phenotype evaluation of eight Chinese probands with Waardenburg syndrome
• A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions
• A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
• A novel <em>KIT</em> mutation in a family with expanded syndrome of piebaldism
• A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features
• A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy
• A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family
• A novel mutation of the StAR gene with congenital adrenal hyperplasia and its association with heterochromia iridis: a case report
• A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV
• A Very Rare Association of Fuchs Heterochromic Uveitis and Ectropion Uvea in Usher Syndrome
• AML presenting with a preleukemic episode and acquired heterochromia in a child with macrosomia
• An Ancient Case of Horner Syndrome?
• Anisometropic amblyopia in a case of type 2 Waardenburg syndrome
• Artistic Iris: A Case of Congenital Sectoral Heterochromia Iridis
• Asymmetric choroidal hypopigmentation in a Son and mother with Waardenburg syndrome type I
• Bilateral asymmetrical partial heterochromia of iris and fundus in Waardenburg syndrome type 2A with a novel <em>MITF</em> gene mutation
• Bilateral cochlear implantation in a child with Waardenburg syndrome: A case report
• Birth palsy in congenital varicella syndrome: A lesson in anatomy
• Cantu syndrome and lymphoedema
• Case Report: A Novel <em>PAX3</em> Mutation Associated With Waardenburg Syndrome Type 1
• Case Report: A Novel Gross Deletion in <em>PAX3</em> (10.26 kb) Identified in a Chinese Family With Waardenburg Syndrome by Third-Generation Sequencing
• Case report: waardenburg syndrome
• Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome
• Clinical and genetic investigation of families with Waardenburg syndrome type 2
• Clinical Insights Into Waardenburg-Shah Syndrome: A Case Series and Literature Review
• Cochlear implantation outcomes in children with Waardenburg syndrome
• Congenital deafness with pigmentary disturbance of the irides
• Congenital horner syndrome with heterochromia iridis associated with ipsilateral internal carotid artery hypoplasia
• Direct-to-consumer DNA testing of 6,000 dogs reveals 98.6-kb duplication associated with blue eyes and heterochromia in Siberian Huskies
• Don't it make my blue eyes brown: heterochromia and other abnormalities of the iris
• Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects
• Eyes of different colours
• Focal cortical dysplasia and heterochromia of the iris
• Forceps trauma in a newborn presenting as iris heterochromia
• Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report
• Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia
• Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II
• Genome-wide association studies for iris pigmentation and heterochromia patterns in Large White pigs
• Girl With Eye Pain and Iris Heterochromia
• Heterochromia and unilateral iris nodules
• Heterochromia following intravitreal chemotherapy in two cases
• Heterochromia irides and mistaken identity of retinoblastoma
• Heterochromia iridis, congenital deafness and skin pigmentary abnormalities: Waardenburg syndrome
• Heterochromia iridis: More than beautiful eyes
• Hétérochromie irienne causée par le syndrome de Waardenburg chez un nourrisson de 2 mois
• Homozygous EDNRB mutation in a patient with Waardenburg syndrome type 1
• Horner's, Heterochromia, and Harlequins
• Identification of a novel mutation of <em>SOX10</em> gene and analysis of the phenotype
• Identification of novel MITF mutations in Chinese families with Waardenburg syndrome type II
• Image of the month: answer: Waardenburg syndrome (WS)
• Iris Heterochromia
• Iris heterochromia and unilateral eyelash hypertrichosis
• Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion
• Iris mammillations: Images and OCT findings
• Iris pigmentation as a quantitative trait: variation in populations of European, East Asian and South Asian ancestry and association with candidate gene polymorphisms
• It is in his eyes
• Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndrome
• Long-term Management of Panuveitis and Iris Heterochromia in an Ebola Survivor
• LONG-TERM OBSERVATION OF MULTIFOCAL METASTATIC INTRAOCULAR CARCINOID WITH ACQUIRED IRIS HETEROCHROMIA
• Managing advanced unilateral pseudoexfoliative glaucoma
• Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations
• Multimodal Ultrawide-Field Imaging Features in Waardenburg Syndrome
• Multiple ocular developmental defects in four closely related alpacas
• Mutational analysis of a Chinese family with oculocutaneous albinism type 2
• New onset of iris heterochromia and a limp
• Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome
• Ophthalmic associations of oculodermal melanocytosis in a tertiary eye hospital in South Asia
• Ophthalmic pathologies in female subjects with bilateralcongenital sensorineural hearing loss
• Oral manifestation of Waardenburg syndrome: a case report and review of the literature
• Pharmacological pseudo-Fuchs
• Phenotypic variability in Waardenburg syndrome resulting from a 22q12.3-q13.1 microdeletion involving SOX10
• Post-thyroidectomy iatrogenic Horner's syndrome with heterochromia
• Presumed ocular juvenile xanthogranuloma and biopsy-proven cutaneous mastocytosis occurring sequentially in a young boy
• Rare causes of childhood leukocoria
• Reversal of Iris Heterochromia in Adult-Onset Acquired Horner Syndrome
• Schlechtes Zeichen: Ein Baby mit verschiedenfarbigen Augen
• Sectoral Heterochromia
• SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis
• Tapioca melanoma of the iris without iris heterochromia
• The Effect of SLT Laser Application on Iris to Treat Sectorial Heterochromia: A Promising Technique
• The Eye Color Experiment: From Berlin to Auschwitz and Back
• The unique association of iris heterochromia with Hermansky-Pudlak syndrome
• Traumatic Cataract and Heterochromia Iridis
• Unilateral straight hair and congenital horner syndrome
• Visual Dermatology: Waardenburg Syndrome Type II
• Waardenburg syndrome
• Waardenburg syndrome
• Waardenburg syndrome
• Waardenburg Syndrome type 1: A case report
• Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris
• Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation
• Waardenburg Syndrome Type I
• Waardenburg syndrome: a rare cause of inherited neuropathy due to SOX10 mutation
• Wardenburg syndrome type 2 in a woman with no genomic mutation commonly associated with the syndrome
• XEN45 Gelstent Implantation in the Treatment of Glaucoma Secondary to Fuchs Uveitis Syndrome