• <em>GDF6</em> Knockdown in a Family with Multiple Synostosis Syndrome and Speech Impairment
• 8 out of 10 patients do well after surgery for tarsal coalitions: A systematic review on 1284 coalitions
• A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability
• A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD)
• A familial case of NOG -related symphalangism spectrum disorder due to a novel NOG variant
• A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss
• A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal
• A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese Family
• A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder
• A novel variant in the ROR2 gene underlying brachydactyly type B: a case report
• A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome
• A Start Codon Variant in <em>NOG</em> Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes
• Analysis of phenotype and pathogenic variants in a Chinese pedigree affected with Multiple synostoses syndrome type 1
• Arthroscopic Calcaneonavicular Coalition and Too-long Anterior Process of the Calcaneus Resection in Children
• Arthroscopic Talocalcaneal Coalition Resection in Children
• Autopsy findings in a stillborn female infant with the Osebold-Remondini syndrome
• Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatment
• BMP antagonists in tissue development and disease
• Child calcaneonavicular coalitions: MRI diagnostic value in a 19-case series
• Clinical observation and genetic analysis of a SYNS1 family caused by novel NOG gene mutation
• Clinical value of combined single photon emission computerized tomography and conventional computer tomography (SPECT/CT) in sports medicine
• Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date
• Double bilateral talocalcaneal and calcaneonavicular coalition in a 15 year-old patient: treatment and results
• Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss
• Genetic and clinical phenotypic analysis of familial stapes sclerosis caused by an NOG mutation
• Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder
• Humeroradial synostosis and the multiple synostosis syndrome: case report
• Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangism
• Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism
• Is the Conductive Hearing Loss in NOG-Related Symphalangism Spectrum Disorder Congenital?
• Multiple synostoses syndrome: Clinical report and retrospective analysis
• Multiple synostoses syndrome: Radiological findings and orthopedic management in a single institution cohort
• Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis
• Natural Progression and Symptomatic Management of Tarsal-Carpal Coalition Syndrome: A Case Report
• Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndrome
• Novel NOG mutation in Japanese patients with stapes ankylosis with broad thumbs and toes
• P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes
• Proximal symphalangism and premature ovarian failure
• Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNB
• Spondylocarpotarsal synostosis syndrome and cervical instability
• Spondylocarpotarsal synostosis syndrome: MRI evaluation of vertebral and disk malformation
• Standard variant venous dysplasia of the cerebellum in a patient suffering from Muenke's syndrome and tinnitus
• Stapedectomy in Teunissen-Cremers Syndrome: Intraoperative Findings and Hearing Outcomes
• Surgical Considerations for Massive Tarsal Coalitions in Multiple Synostosis Syndrome: A Case Report
• Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene
• Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene
• Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism
• Talocalcaneal Tarsal Coalition Size: Evaluation and Reproducibility of MRI Measurements
• Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a family
• Tarsal tunnel syndrome in a patient on long-term peritoneal dialysis: case report
• Tarsal-carpal coalition syndrome: a familial case
• Tarsal-carpal coalition syndrome: importance of early diagnosis
• Tarsal-carpal coalition syndrome: Report of a novel missense mutation in NOG gene and phenotypic delineation
• Temporal Bone Histopathology in NOG-Symphalangism Spectrum Disorder
• The multiple synostoses syndrome. A plea for simplicity
• Variable phenotypes of multiple synostosis syndrome in patients with novel NOG mutations
• Wrist denervation in isolation: a prospective outcome study with patient selection by wrist blockade