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Research 871–900 of 1000+
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Congenital atrichia associated with situs inversus and mesocardia
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Assessment of the Embryological Origin, Anatomical and Histological Structure of the Skin
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co- option in the evolution of the hair follicle
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Acquired Uncombable Hair
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver
- Diagnosis and management of hair loss in children
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hypotrichosis due to short anagen
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Secondary cicatricial and other permanent alopecias
- Hair Shaft Dysplasias
- Hair loss
- Disease causing homozygous variants in the human hairless gene
- Hair loss in children.
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Cronkhite-Canada Syndrome: A Case Report
- Diagnosis of Scalp Disorders using Machine Learning and Deep Learning Approach -- A Review
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Perspectives on Dermatopathology
- A Review on Herbal Drugs Used For Hair Growth Promotion
- Role of Insulin Resistance and Oxidative Stress in Hair Loss
- Two females with hair loss
- Abnormal fingerprints and immigration delay disease