Loucks, C. M., Parboosingh, J. S., Shaheen, R., Bernier, F. P., McLeod, D. R., Seidahmed, M. Z., . . . Innes, A. M. (2015). Matching two independent cohorts validates DPH1 as a gene responsible for autosomal recessive intellectual disability with short stature, craniofacial and ectodermal anomalies. Hum Mutat.
Citación estilo ChicagoLoucks, Catrina M., et al. "Matching Two Independent Cohorts Validates DPH1 As a Gene Responsible for Autosomal Recessive Intellectual Disability With Short Stature, Craniofacial and Ectodermal Anomalies." Hum Mutat 2015.
Cita MLALoucks, Catrina M., et al. "Matching Two Independent Cohorts Validates DPH1 As a Gene Responsible for Autosomal Recessive Intellectual Disability With Short Stature, Craniofacial and Ectodermal Anomalies." Hum Mutat 2015.