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- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Prediction of male-pattern baldness from genotypes
- British Society for Dermatopathology
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- BIPHENOTYPIC LEUKAEMIA
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Genetics of Structural Hair Disorders
- Cutaneous signals of immune system disease
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Trans‐species hair growth induction by human hair follicle dermal papillae
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- E-Poster
- PRMT5 inhibition has a potent anti-tumor activity against adenoid cystic carcinoma of salivary glands
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases