• A 15-year Follow-Up of a Gingivectomy Procedure for Idiopathic Gingival Fibromatosis: A Case Report and Literature Review
• A case of Zimmermann-Laband syndrome with supernumerary teeth
• A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1
• A novel gene <em>ZNF862</em> causes hereditary gingival fibromatosis
• A novel gene ZNF862 causes hereditary gingival fibromatosis
• A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3
• A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15
• A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management
• Autosomal recessive gingival fibromatosis with distinctive facies
• Case report: Rutherfurd syndrome associated with Marfan syndrome
• Cherubism combined with epilepsy, mental retardation and gingival fibromatosis (Ramon syndrome): a case report
• Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review
• Clinically Relevant <em>KCNQ1</em> Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca²⁺ Sensitivity of the Channel
• Clinics and genetic background of hereditary gingival fibromatosis
• Current concepts on gingival fibromatosis-related syndromes
• Early onset of hereditary gingival fibromatosis in a 28-month-old
• Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G &gt; A (p.R357Q) variant
• Evidence of genetic heterogeneity for hereditary gingival fibromatosis
• Extensive Gingival Enlargement in Siblings: A case report
• Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome
• Familial gingival fibromatosis associated with progressive deafness in five generations of a family
• Familial gingival fibromatosis; no correlation with HLA-antigen. A family study
• Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis
• Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes
• Genetic heterogeneity of gingival fibromatosis on chromosome 2p
• Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21
• Genome-wide expression analysis of hereditary hyperplastic gingivitis in silver foxes (Vulpes vulpes) using canine microarrays
• Genomic analysis of gum disease and hypertrichosis in foxes
• Gingival fibromatosis with sensorineural hearing loss: an autosomal dominant trait
• Gingival fibromatosis: clinical, molecular and therapeutic issues
• Gingival fibromatosis: study of three generations with consanguinity
• Gingival overgrowth in children: epidemiology, pathogenesis, and complications. A literature review
• Gummy smile: could it be genetic? Hereditary gingival fibromatosis
• Hereditary generalized gingival fibromatosis associated with hypertrichosis: report of five cases in one family
• Hereditary gingival fibromatosis
• Hereditary Gingival Fibromatosis and Developmental Anomalies: A Case Report
• Hereditary gingival fibromatosis associated with generalized aggressive periodontitis: a case report
• Hereditary gingival fibromatosis associated with hearing loss and supernumerary teeth--a new syndrome
• Hereditary gingival fibromatosis in children: a systematic review of the literature
• Hereditary gingival fibromatosis with a recessive mode of inheritance. Case reports
• Hereditary gingival fibromatosis with distinctive facies
• Hereditary gingival fibromatosis--a review
• Hereditary gingival fibromatosis: aggressive 2-stage surgical resection in lieu of traditional therapy
• Hereditary gingival fibromatosis: clinical and ultrastructural features of a new family
• Hereditary gingival fibromatosis: report of a five-generation family using cellular proliferation analysis
• Hereditary gingival fibromatosis: report on three families and dermatoglyphic analysis
• Hereditary gingival fibromatosis. Report of an extensive four-generation pedigree
• Heterogeneity in the gingival fibromatoses
• Hypertrichosis universalis congenita: a separate entity, or the same disease as gingival fibromatosis?
• Idiopathic gingival fibromatosis and primary analysis of dominant bacteria in subgingival biofilm: a case report
• Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations
• New evidence of genetic heterogeneity causing hereditary gingival fibromatosis and ALK and CD36 as new candidate genes
• Non-familial cherubism: A case report with its surgical management
• Nonsyndromic Gingival Fibromatosis: A Rare Case Report
• Nonsyndromic hereditary gingival fibromatosis: Characterization of a family and review of genetic etiology
• Novel <em>REST</em> Truncation Mutations Causing Hereditary Gingival Fibromatosis
• Novel REST Truncation Mutations Causing Hereditary Gingival Fibromatosis
• Ramon Syndrome- A Rare Form of Cherubism
• RARE CASE OF IDIOPATHIC GINGIVAL FIBROMATOSIS AFFECTING PRIMARY DENTITION
• Refinement of the GINGF3 locus for hereditary gingival fibromatosis
• Refinement of the locus for autosomal dominant hereditary gingival fibromatosis (GINGF) to a 3.8-cM region on 2p21
• REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis
• Sequence analysis of the Ras-MAPK pathway genes SOS1, EGFR &amp; GRB2 in silver foxes (Vulpes vulpes): candidate genes for hereditary hyperplastic gingivitis
• Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K⁺ channelopathies
• Syndromic gingival fibromatosis
• The Autosomal Dominant Inheritance of Hereditary Gingival Fibromatosis: A Case Report
• The Role of <em>KCNQ1</em> Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome
• Treatment and long-term follow-up of a patient with hereditary gingival fibromatosis: a case report
• Treatment of a patient with hereditary gingival fibromatosis: a case report
• Ultrastructural aspects of connective tissue in hereditary gingival fibromatosis
• Wide clinical spectrum in Zimmermann-Laband syndrome
• Zimmerman-Laband syndrome and profound mental retardation
• Zimmermann-Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions
• Zimmermann-Laband syndrome in a patient with severe mental retardation
• Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis
• Zimmermann-Laband syndrome: Clinical and cytogenetic study in two related patients
• Zimmermann-Laband syndrome: further clinical delineation