Gemini Syndrome,Lorier Gemini Worn & Wound Collaboration – Windup Watch Shop,Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati–Engelmann disease type II | Journal of Human Genetics,Frontiers | Variants of SLC39A4 cause acrodermatitis enteropathica in Tibetan, Yi, and Han families in Sichuan region of southwestern China: a case report series,A rare haplotype of the GJD3 gene segregating in familial Meniere's disease interferes with connexin assembly | Genome Medicine | Full Text,