Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3
Pediatric Research2017Vol. 82(5), pp. 753–758
Citations Over TimeTop 10% of 2017 papers
Muhammad Umair, Bader Alhaddad, Afzal Rafique, Abid Jan, Tobias B. Haack, Elisabeth Graf, Asmat Ullah, Farooq Ahmad, Tim M. Strom, Thomas Meitinger, Wasim Ahmad
Related Papers
- → Osteogenesis Imperfecta(2017)22 cited
- → Costovertebral anomalies in osteogenesis imperfecta(1985)16 cited
- → Severe osteogenesis imperfecta: new therapeutic options?(2001)13 cited
- Benefits of Pamidronate Treatment in Osteogenesis Imperfecta(2005)
- → Osteogenesis imperfecta type 1(2020)