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- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Letter from Brisbane [Letters to editor]
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Interactions between epidermal growth factor and the <i>Tabby</i> mutation in skin
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
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