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Research 451–480 of 1000+
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Acne Syndromes and Mosaicism
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Current Genetics in Hair Diseases
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- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Ehlers-Danlos syndrome: From bedside to bench
- Bachmann–Bupp syndrome and treatment
- Oral Presentation Abstracts
- Short Peptides Induce Development of Root Hair Nicotiana tabacum
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Hdac1 and Hdac2 regulate the quiescent state and survival of hair-follicle mesenchymal niche
- Pachyonychia congenita: Sporadic onset with mutation analysis
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion