• <em>ALX</em>-Related Frontonasal Dysplasias: Clinical Characteristics and Surgical Management
• <em>Alx1</em> Deficient Mice Recapitulate Craniofacial Phenotype and Reveal Developmental Basis of <em>ALX1</em>-Related Frontonasal Dysplasia
• 50 Years Ago in TheJournalofPediatrics: Understanding the Genetic Basis of Frontonasal Dysplasia
• A Diagnostic Conundrum: Ectopic Nasal Ossification, Submucosal Alveolar Cleft, Absent Posterior Atlantal Arch, and Corpus Callosum Lipoma
• A Family with Craniofrontonasal Syndrome and a Mutation (p.G151S) in the EFNB1 Gene: Expanding the Phenotype
• A long-term evaluation of 150 costochondral nasal grafts
• A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene
• A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication
• A Novel Missense Variant in the <em>ALX4</em> Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family
• A Novel Missense Variant in the ALX4 Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family
• A rare homozygous ALX4 mutation in a Bangladeshi girl with frontonasal dysplasia type-2 (FND2)
• Absence of nasal bone and brachydactyly: a probable new familial syndrome
• Addressing hypertelorism: Indications and techniques
• Alx1 Deficient Mice Recapitulate Craniofacial Phenotype and Reveal Developmental Basis of ALX1-Related Frontonasal Dysplasia
• ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration
• ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration
• Anterior interhemispheric calcified lipoma together with subcutaneous lipoma and agenesis of corpus callosum: a rare manifestation of midline craniofacial dysraphism
• Aristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats
• Bifid nose - a mild degree of frontonasal dysplasia. A case report
• BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome
• Case report: Craniofrontonasal syndrome caused by a novel variant in the <em>EFNB1</em> gene in a Colombian woman
• Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes
• Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patients
• Clinical Features and Management of a Median Cleft Lip
• Clover-shaped advancement flap for correction of short and broad columella in a patient with frontorhiny
• Computer-Assisted Surgery in Facial Bipartition Surgery
• Correction of nasal tip deformity using an island flap of nasal dorsum
• Correction of severe bifid nose deformity using an open W-shaped incision
• Costochondral Grafting for Nasal Airway Reconstruction in an Infant With Frontonasal Dysplasia
• Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment
• Crucial and Overlapping Roles of Six1 and Six2 in Craniofacial Development
• Cumulative inactivation of Nell-1 in Wnt1 expressing cell lineages results in craniofacial skeletal hypoplasia and postnatal hydrocephalus
• De novo ZIC2 frameshift variant associated with frontonasal dysplasia in a Limousin calf
• Designing custom three-dimensional printed eyeglasses for children with frontonasal abnormalities: addressing challenges in access and fit
• Diagnostic criteria in Pai syndrome: results of a case series and a literature review
• Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4
• Etiology and genetic factors in clefts of lip and/or palate reported at children's hospital, Lahore, Pakistan
• Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis
• Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny
• Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia
• Facial clefts and facial dysplasia: revisiting the classification
• Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndrome
• Frontonasal and fibrous dysplasia in a patient with unilateral cleft lip and palate
• Frontonasal dysplasia with severe occipital lobe hypoplasia
• Frontonasal dysplasia: A case report
• Frontonasal Dysplasia: A Diagnostic Challenge with Fetal MRI in Twin Pregnancy
• Frontonasal dysplasia: oral features, restorative and orthodontic dental treatment in a child
• Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology
• Frontonasal fold thickness-to-nasal bone length ratio as a prenatal sonographic marker for trisomy 21 in a low-risk population
• Generation and characterization of Six2 conditional mice
• Genes Related to Frontonasal Malformations Are Regulated by miR-338-5p, miR-653-5p, and miR-374-5p in O9-1 Cells
• Hospitalizations from Birth to 28 Years in a Population Cohort of Individuals Born with Five Rare Craniofacial Anomalies in Western Australia
• Hydroxyapatite implantation for the repair of a congenital nasal anomaly: 10 years follow-up
• Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2
• Images in anesthesiology: facemask ventilation with a frontonasal encephalocele
• INTERMITTENT EXOTROPIA COURSE IN FRONTONASAL DYSPLASIA AND SEVERE ORBITAL HYPERTELORISM: CASE REPORT
• Lineage-specific requirements of Alx4 function in craniofacial and hair development
• Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans
• Loss of ephrinB1 in osteogenic progenitor cells impedes endochondral ossification and compromises bone strength integrity during skeletal development
• Maternal SLE and brachytelephalangic chondrodysplasia punctata in a patient with unrelated de novo RAF1 and SIX2 variants
• Medial Femoral Condyle Free Flap for Premaxillary Reconstruction in Median Facial Dysplasia
• Median cleft of the upper lip: A new classification to guide treatment decisions
• Nasal Reconstruction of a Frontonasal Dysplasia Deformity Using Aesthetic Rhinoplasty Techniques
• Nasal Reconstruction of a Frontonasal Dysplasia via Septal L-Strut Reconstruction Using Costal Cartilage
• Neurological picture. Bitemporal hemianopsia in frontonasal dysplasia, callosal agenesis, basal meningocele and eye abnormalities
• Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele
• Ocular Manifestations of Frontonasal Dysplasia
• Ocular Morbidity in the Correction of Orbital Hypertelorism and Dystopia: A 15-Year Experience
• Oculo-Auriculo-Fronto-Nasal Syndrome With Duane Retraction Syndrome and Dysplastic Bony Structure in the Midline of Nose
• Oculoauriculofrontonasal Dysplasia Syndrome With Additional Clinical Features
• Oculoauriculofrontonasal syndrome: case series revealing new bony nasal anomalies in an old syndrome
• Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review
• Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndrome
• Orthognathic Surgery and Rhinoplasty to Address Nasomaxillary Hypoplasia
• Pagetoid polyostotic fibrous dysplasia
• Pai syndrome: a review
• Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype
• Prenatal diagnosis of a severe form of frontonasal dysplasia with severe limb anomalies, hydrocephaly, a hypoplastic corpus callosum, and a ventricular septal defect using 3D ultrasound: a case report and literature review
• Prenatal diagnosis of frontonasal dysplasia associated with bilateral periventricular nodular heterotopia
• Prenatal diagnosis of frontonasal dysplasia with anterior encephalocele
• Prenatal diagnosis of isolated frontonasal dysplasia: A case report
• Reconstruction of the shortened columella in mild bifid nose using a propeller flap based on the nasal columella artery
• Rhinoplasty in a 3 Week Old: Surgical Challenges in the Setting of Severe Congenital Frontonasal Dysplasia
• SIX2 gene haploinsufficiency leads to a recognizable phenotype with ptosis, frontonasal dysplasia, and conductive hearing loss
• Structural Rhinoplasty as an Effective Surgical Approach for Frontonasal Dysplasia
• Surgical Correction of a Bifid Nose Deformity with a Split M-Shaped Flap
• Surgical Management of a Mild Case of Frontonasal Dysplasia: A Case Report and Review of Literature
• Surgical Strategies for Soft Tissue Management in Hypertelorbitism
• TFAP2 paralogs regulate midfacial development in part through a conserved <em>ALX</em> genetic pathway
• TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathway
• The oculoauriculofrontonasal syndrome: Further clinical characterization and additional evidence suggesting a nontraditional mode of inheritance
• The relationship between external bony defects and widened lateral interorbital distance in frontoethmoidal encephalomeningocele
• The value of three-dimensional printing modelling for surgical correction of orbital hypertelorism
• Tooth Abnormalities and Occlusal Disorders in Individuals With Frontonasal Dysplasia
• Toward clinical and molecular dissection of frontonasal dysplasia with facial skin polyps: From Pai syndrome to differential diagnosis through a series of 27 patients
• Trio-Based Whole-Exome Sequencing Identifies a <em>De novo EFNB1</em> Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay
• Two novel mutations within FREM1 gene in patients with bifid nose
• Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation
• Zebrafish models of alx-linked frontonasal dysplasia reveal a role for Alx1 and Alx3 in the anterior segment and vasculature of the developing eye
• Zebrafish zic2 controls formation of periocular neural crest and choroid fissure morphogenesis