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Research 31–60 of 1000+
- Alopecia Areata: A Review of the Genetic Variants and Immunodeficiency Disorders Associated with Alopecia Areata
- For early diagnosis of young patients with Werner syndrome: Indication for genetic testing
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- New clinico‐genetic classification of trichothiodystrophy
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- Comparative Analysis of Chloroplast Genomes in Sansevieria Reveals Phylogenetic Relationships and High Variability Molecular Markers
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- Reciprocal effects suggest maternal and extranuclear influences on fruit traits in winter squash breeding
- Inherited Hair Disorders
- Frontal fibrosing alopecia: reflections and hypotheses on aetiology and pathogenesis
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Premature hair graying: a multifaceted phenomenon
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- The Pathobiology of Skin Aging
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- The First Visit: Consult and Workup Before Sperm Banking
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- The Contribution of Endogenous and Exogenous Factors to Female Alopecia
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Monilethrix, a rare inherited hair shaft disorder in siblings