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Research 181–210 of 1000+
- Netherton Syndrome
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Inherited Acrodermatitis Enteropathica
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Trichothiodystrophy in a child with occult learning disorder
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- Congenital adrenal hyperplasia
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Perspectives of Kennedy's disease
- Nonclassic adrenal hyperplasia
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Werner′s syndrome
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations