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Research 241–270 of 1000+
- Molecular Genetics of Alopecias
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report
- Serum markers thrombophilia in pregnant women with Systemic Lupus Erythematosus
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Pathology in Practice
- Serine palmitoyltransferase and peripheral neuropathy: studies on neuropathy-causing mutations and their biochemical hallmarks
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Female Androgenetic (?) Alopecia
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Alopecia X em cães: revisão
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Monilethrix: Beaded hair and hypotrichosis in a child
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Rates of polycystic ovary syndrome (PCOS) symptoms in relatives of patients with PCOS
- What Ages Hair?
- Factors affecting the development of alopecia areata in children
- Biology and Genetics of Hair
- Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Monilethrix
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Hypothyroidism in Dogs
- [Netherton's syndrome in two sisters].