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- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Monilethrix
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Biology and Genetics of Hair
- Alopezien und Hypotrichosen im Kindesalter
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Current Genetics in Hair Diseases
- Clinical Snippets
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Clinical Snippets
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Monilethrix: A rare hereditary condition
- Woolly Antics between the Sheaths
- Monilethrix – Case report of a rare disease
- Monilethrix in three generations
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Alopecia in a 19-Month-Old Boy
- Inherited Disorders of the Hair