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Research 211–240 of 1000+
- Inherited Hair Disorders
- Identification and characterization of genes for skin and hair disorders
- Disorders of Hair Pigmentation
- Dermatological diseases from a genetic perspective
- Disorders linked to insufficient androgen action in male children
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Psoriasis and Related Disorders
- Hair shaft disorders
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- 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
- Androgenetic alopecia: An autosomal dominant disorder
- Pigmentary and Hair Disorders
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- Zebrafish Model of Hereditary Pigmentary Disorders
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Managing Cutaneous Manifestations of Hyperandrogenic Disorders
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Identificación de la variación molecular y genética subyacente a las enfermedades de la piel
- Lifestyle changes and Nutrition in Polycystic Ovarian Disorder: A Holistic Review
- Dermatologic Disorders
- Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
- Table 2_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Disorders of Keratinization
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Melasma and Endocrine Disorders