Disease: Fibromatosis gingival hypertrichosis
- 'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes
- "Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes
- A rare case of gingival fibromatosis associated with hypertrichosis and a dysmorphic face
- A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management
- Ambras syndrome: A rare case report
- Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres
- Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants
- Cherubism combined with epilepsy, mental retardation and gingival fibromatosis (Ramon syndrome): a case report
- Cherubism, gingival fibromatosis, epilepsy, and mental deficiency (Ramon syndrome) with juvenile rheumatoid arthritis
- Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review
- Collagen synthesis in idiopathic and dilantin-induced gingival fibromatosis
- Congenital Generalized Hypertrichosis, Gingival Hyperplasia, a Coarse Facies with Constriction Bands: A Rare Association
- Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes
- Current concepts on gingival fibromatosis-related syndromes
- De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features
- Delineating the 17q24.2-q24.3 microdeletion syndrome phenotype
- ELMO2 biallelic pathogenic variants in a patient with gingival hypertrophy and cherubism phenotype: Case report and molecular review
- Enamel Renal Syndrome: A Systematic Review
- Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome
- Familial microdeletion of 17q24.3 upstream of SOX9 is associated with isolated Pierre Robin sequence due to position effect
- Fibromatosis gingivae
- Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca<sup>2+</sup>-Activated K<sup>+</sup> Channel SK3 Cause Zimmermann-Laband Syndrome
- Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes
- Genomic analysis of gum disease and hypertrichosis in foxes
- Gingival fibromatosis
- Gingival fibromatosis with congenital hypertrichosis
- Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome
- Gingival fibromatosis with hypertrichosis. A case report
- Gingival fibromatosis, mental retardation, epilepsy and hypertrichosis
- Hereditary generalized gingival fibromatosis associated with hypertrichosis: report of five cases in one family
- Hereditary gingival fibromatosis (HGF) with hypertrichosis is unlinked to the HGF1 and HGF2 loci
- Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome
- Hereditary gingivo-fibromatosis
- Heterogeneity in gingival fibromatosis
- Heterogeneity in gingival fibromatosis
- Heterogeneity in the gingival fibromatoses
- Homozygous mutation in ELMO2 may cause Ramon syndrome
- Hypertrichosis universalis congenita: a separate entity, or the same disease as gingival fibromatosis?
- Idiopathic familial gingival fibromatosis associated with mental retardation, epilepsy and hypertrichosis
- Idiopathic gingival fibromatosis associated with mild hypertrichosis
- Long-term management of an idiopathic gingival fibromatosis patient with the primary dentition
- Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in utero
- Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
- Oral and dental abnormalities in Barber-Say syndrome
- Patients with <em>KCNH1</em>-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome
- Ramon Syndrome- A Rare Form of Cherubism
- Resection of Gingival Fibromatosis with High-power Laser
- Retinal changes and tumorigenesis in Ramon syndrome: follow-up of a Brazilian family
- Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition?
- Syndromes with gingival fibromatosis: A systematic review
- Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K<sup>+</sup> channelopathies
- The phenotypic overlap of syndromes associated with hereditary gingival fibromatosis: follow-up of a family for five years
- The Zimmermann-Laband syndrome
- What syndrome is this? Gingival fibromatosis-hypertrichosis syndrome
- Wide clinical spectrum in Zimmermann-Laband syndrome
- Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant
- Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis
- Zimmermann-Laband syndrome: further clinical delineation