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Research 31–60 of 1000+
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Congenital Adrenal Hyperplasia
- Nonclassic congenital adrenal hyperplasia
- Congenital adrenal hyperplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Congenital atrichia and hypotrichosis
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Dermatopathology and molecular genetics
- Disorders of hair in children
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Diseases of Periocular Hair
- Hair and scalp disorders
- Hirsutism: diagnosis and treatment
- Congenital hair loss disorders: Rare, but not too rare
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Atlas of Geriatric Dermatology
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Genetics of Alopecia
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Genetic Hair Disorders: A Review