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Research 391–420 of 606
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Acute vesiculobullous hand dermatitis and anagen effluvium in Ganoderma lucidum-induced aplastic crisis
- Pigmentary mosaicism: An update
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- GRowing an Epidermal Tumor
- Werner′s syndrome
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Eleven pairs of Japanese male twins suggest the role of epigenetic differences in androgenetic alopecia
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Case Report: Rare aplastic anemia in pediatric systemic lupus erythematosus: a case series and systematic literature review
- Older age and low testosterone levels are independently associated with kidney stone prevalence in men: results from a large cross-sectional study
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Drug-associated gingival disorders: a retrospective pharmacovigilance assessment using disproportionality analysis
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association