Search
for
Sort by
Research 991–1000 of 1000+
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Recently Identified Forms of Epidermolysis Bullosa
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Hair Keratin
- The Effect of a Food Supplement and a Hair Lotion on the Progression of Androgenetic Alopecia
- Epidemiological Analysis of Alopecia in Migrant Communities at Dr. Hair™ Clinics
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- The Frontal Fibrosing Alopecia Treatment Dilemma
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14