Cite
MLA Citation
Luisa Mackenroth et al.. “An overlapping phenotype of Osteogenesis imperfecta and Ehlers–Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing.” American journal of medical genetics, vol. 170, no. 4, 2016, pp. 1080–1085. http://access.bl.uk/ark:/81055/vdc_100031198014.0x00004a