• 3-D COSMOS: a new 3-D model based computerised operation simulation and navigation system
• 3-D imaging of the facial surface by topometry using projected white light strips
• A case of rare isolated agnathia and literature review
• A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
• A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome
• A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1
• Agnathia-otocephaly complex: a case report and examination of the OTX2 and PRRX1 genes
• Airway management during an EXIT procedure for a fetus with dysgnathia complex
• Attitudes Toward Domestic Violence and Corporal Punishment Among Former Soviet Union Immigrants in Israel
• Auriculo-condylar syndrome
• Auriculo-condylar syndrome is associated with highly variable ear and mandibular defects in multiple kindreds
• Auriculo-condylar syndrome or new syndrome?
• Auriculo-condylar syndrome: additional patients
• Auriculo-condylar syndrome: further evidence for a new disorder
• Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity
• Auriculo-condylar syndrome. Confronting a diagnostic challenge
• Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants
• Auriculocondylar syndrome: Pathogenesis, clinical manifestations and surgical therapies
• Autosomal dominant isolated question mark ear
• Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant
• Clinical and magnetic resonance findings in the temporomandibular joints of patients before and after orthognathic surgery
• Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome
• Complete mouth rehabilitation after transposition osteotomy based on intraoral scanning: an experimental approach
• Computed tomographic reconstruction of a fetus with the dysgnathia complex (agnathia-otocephaly)
• Dominant-negative Gα subunits are a mechanism of dysregulated heterotrimeric G protein signaling in human disease
• Dysgnathia complex sine holoprosencephaly nor synotia: a case report and discussion of its nosology
• Dysgnathia complex, a rare deviation
• Early childhood temperament predicts substance use in young adults
• Focus Issue: New insights in GPCR to G protein signaling
• Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
• Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases
• Further phenotypic delineation of the auriculocondylar syndrome type 2 with literature review
• Genetic factors in isolated and syndromic laryngeal cleft
• Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome
• Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses
• Loss-of-function of Endothelin receptor type A results in Oro-Oto-Cardiac syndrome
• Mandibular distraction osteogenesis as first step in the early treatment of severe dysgnathia in childhood
• Microtia, severe micrognathia and absent ossicles: auriculo-condylar syndrome or new entity?
• Muscle function therapy of the orofacial area
• Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
• Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects
• New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving <em>TWIST1</em> regulatory elements
• Novel features in auriculo-condylar syndrome
• Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
• Ossicular fusion and cholesteatoma in auriculo-condylar syndrome: in vivo evidence of arrest of embryogenesis
• Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2
• OTX2 mutations contribute to the otocephaly-dysgnathia complex
• PAN-AMPK activator O304 improves glucose homeostasis and microvascular perfusion in mice and type 2 diabetes patients
• Preferences for treatment among adolescents with Type 1 diabetes: a national study using a discrete choice experiment model
• Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report
• Public Knowledge and Attitudes Regarding the Use of Antibiotics and Resistance: Findings from a Cross-Sectional Study Among Palestinian Adults
• Question mark ears and post-auricular tags
• Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?
• Respiratory and gastrointestinal dysfunctions associated with auriculo-condylar syndrome and a homozygous PLCB4 loss-of-function mutation
• Sibling number and prevalence of allergic disorders in pregnant Japanese women: baseline data from the Kyushu Okinawa Maternal and Child Health Study
• Subjective evaluation of the accuracy of video imaging prediction following orthognathic surgery in Chinese patients
• Surgical Approach in a Patient With Agnathia-Otocephaly Complex: Three-Stage Mandibular Distraction Protocol
• Surgical options for treatment of snoring and sleep apnea
• Surgical visual treatment objective: cephalometric planning in the treatment of dysgnathia of facial complex
• Syndromes of the first and second branchial arches, part 2: syndromes
• Syndromes of the first and second pharyngeal arches: A review
• Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
• The association between Helicobacter pylori and laryngopharyngeal reflux in laryngeal pathologies
• The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
• The correction of auricular and mandibular deformities in auriculo-condylar syndrome
• The Partnership of Medical Genetics and Oral and Maxillofacial Surgery When Evaluating Craniofacial Anomalies
• Three-dimensional registration of the facial surface using projected white light stripes (TRICOLITE - triangulation with coded light technique)
• Transmission of the dysgnathia complex from mother to daughter
• Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies