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- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Congenital atrichia and hypotrichosis
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- AAPS and PSRC 2016 Abstract Supplement
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Management of Serious Adverse Events Following Deoxycholic Acid Injection for Submental and Jowl Fat Reduction: A Systematic Review and Management Recommendations
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Late Management of Burns
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Hair loss after covid 19 - case series
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Oral Manifestations of Hematologic and Nutritional Diseases
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- How to diagnose a lipodystrophy syndrome
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Biology of Hair Growth
- Yellow and orange in cutaneous lesions: clinical and dermoscopic data
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Platelet-rich fibrin in the management of oral mucosal lesions: a scoping review
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent