Fig. 1
From: Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV
The neonatal X-ray showed deformity in the long bones, consistent with in utero fractures.
Fig. 1 | Human Genome Variation
From: Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV
The neonatal X-ray showed deformity in the long bones, consistent with in utero fractures.
