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- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Pure Hair‐Nail Ectodermal Dysplasia: Expanding the HOXC13 Genotypic Spectrum
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Hair and Nail Relationship
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Current Genetics in Hair Diseases
- N02. Hair and Nails
- Keratin disorders: from gene to therapy
- Clouston’s syndrome: a rare case report
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- El teorema del 0,7 o el otro teorema de Pitágoras
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Genetic hair and nail disorders
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- A new type of pachyonychia congenita.