Abstracts: Genetics and Genodermatoses
Genetics and Genodermatoses
- A novel monilethrix mutation in the in Coil 2 of K86 causing autosomal dominant monilethrix with incomplete penetrance
- A novel mutation in the human hairless transcript gene in a family with Marie Unna hereditary hypotrichosis
- Analysis of family factors according to basic and specific (BASP) classification in Korean androgenetic alopecia patients : Multicenter study of the Korean Hair Research Society
- Association between estrogen receptor beta gene (ESR2) polymorphisms and female pattern hair loss – more evidence for a detrimental role for estrogens in hair growth
- Common variants in the Trichohyalin gene are associated with straight hair in Europeans
- Congenital generalized hypertrichosis is a genomic disorder
- Epidemiology of folliculitis decalvans and keratosis follicularis spinulosa decalvans in British Columbia
- Estimation of finasteride effect on androgenic alopecia patients by determination of the triplet repeat number in androgen receptor gene and androgenic hormones in serum
- H Syndrome – an Autosomal Recessive Genodermatosis with Hypertichosis as a Prominent Feature
- Keratin 74 is a novel determinant of human hair texture and is mutated in autosomal dominant woolly hair
- Mutations in WNT10A lead to the odonto-onycho-dermal dysplasia syndrome – the first Australian case
- Research of mutation of type II hair keratin gene in a pedigree of monilethrix
12 abstracts