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Research 331–360 of 1000+
- Alopezien und Hypotrichosen im Kindesalter
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Marie-unna hereditary hypotrichosis
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Diagnosis and Management of Melanoma of the Scalp: A Review of the Literature
- Clinical Impact of Molecular Diagnostics in Endocrinology
- Woolly Antics between the Sheaths
- Effect of gamma-ray exposure on the genome-editing efficiency of improved genome-editing via oviductal nucleic acids delivery (<i>i</i>-GONAD)
- PA05 A rare case of cardiocutaneous syndrome in a young child
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Gene Variant in Amish a Clue to Better Aging
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Gene that causes woolly hair revealed
- Hair Today
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Characterization of an autoimmune condition associated with AEC syndrome
- The long and the short of it: evidence that <i>FGF5</i> is a major determinant of canine ‘hair’‐itability
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Genome‐wide association study identifies variants associated with hair length in Brangus cattle
- Hox in the Niche Controls Hairy-geneity
- [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis].
- O04 HPV8 E6 leads to Lrig1+ keratinocyte stem cell expansion
- Alopecia totalis in an infant
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- 40 PRLR and PCCA variants associated with hair length in Brangus heifers
- Congenital hair loss disorders: Rare, but not too rare
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- The dermatological consequences of obesity
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix