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Research 31–60 of 1000+
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Current evaluation of amenorrhea
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Acne
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- The Genetics of Acne
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Ichthyosis with confetti: clinics, molecular genetics and management
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- CURRENT UNDERSTANDING OF VITILIGO: A COMPREHENSIVE LITERATURE REVIEW
- Commentary 2
- New developments in the molecular treatment of ichthyosis: review of the literature
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Claves diagnósticas en displasias pilosas II
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Pathways to inflammation: acne pathophysiology
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Inherited Disorders of the Hair
- Congenital atrichia and hypotrichosis
- Biotinidase deficiency characterized by skin and hair findings
- Adrenal causes of endocrine hypertension in childhood or adolescence
- 9 Pilosebaceous physiology in relation to hirsutism and acne