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Research 31–60 of 1000+
- Two parietal cephaloceles in a female neonate
- SUN-069 A 14 Year Old Female with Primary Amenorrhea
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Index of Suspicion
- Clinical Corner: Case Report Spermatozoa and Chronic Treatment with Finasteride: A TEM and FISH Study
- Congenital atrichia with papular lesions
- Depression from a physical symptom.
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Congenital Atrichia: A Case Report
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- THE PATHOGENESIS OF ALOPECIA AREATA
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Clinical relevance of hair microscopy in alopecia