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Research 151–180 of 347
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Bloom's syndrome–‐a first report from India
- Tabby pattern genetics – a whole new breed of cat
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Siberian cats help in solving part of the mystery surrounding golden cats
- Current Status of Hair Restoration Surgery
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Congenital atrichia with papular lesions
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Hair That Is Difficult to Manage in a Hispanic Girl
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report