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Research 31–60 of 1000+
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Congenital atrichia and hypotrichosis
- Masquerading of trichotillomania in a family with monilethrix
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Ugreelig hår
- Pathology in Practice
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Edar Signaling in the Control of Hair Follicle Development
- Hair and Nail Relationship
- Approach to Alopecia in Dogs in Clinical Practice
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Keratin disorders: from gene to therapy
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Ectodysplasin research—Where to next?
- Research Snippets
- Scaling dermatosis in three dogs associated with abnormal sebaceous gland differentiation
- 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
- Alopecia Areata with Renal Dysgenesis
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- A new type of pachyonychia congenita.