Search
for
Sort by
Research 31–60 of 1000+
- Familial Nonmembranous Aplasia Cutis of the Scalp
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Spangled hair in siblings
- Monilethrix
- Familial congenital generalized hypertrichosis
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Short anagen hair syndrome
- Eruptive Vellus Hair Cyst
- Monilethrix
- Monilethrix in three generations
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Acquired uncombable hair
- Disorders of pigmentation in infants and children
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Alopecia frontal fibrosante: revisão bibliográfica dos aspectos gerais, fisiopatológicos, diagnósticos e do tratamento
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- Pearly Pinna Papules in a Young Female
- Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day!
- Two females with hair loss
- Monilethrix – Case report of a rare disease
- Monilethrix with Acitretin
- A University Center for the Performing Arts
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Marie-unna hereditary hypotrichosis
- Keratosis follicularis spinulosa decalvans in a family