Works matching DE "POP11 (Computer program language)"

Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia.

Published in:

Clinical Genetics, 2017, v. 92, n. 1, p. 91, doi. 10.1111/cge.12964

By:

• Barraza‐García, J.;
• Rivera‐Pedroza, C.I.;
• Hisado‐Oliva, A.;
• Belinchón‐Martínez, A.;
• Sentchordi‐Montané, L.;
• Duncan, E.L.;
• Clark, G.R.;
• del Pozo, A.;
• Ibáñez‐Garikano, K.;
• Offiah, A.;
• Prieto‐Matos, P.;
• Cormier‐Daire, V.;
• Heath, K.E.

Publication type:

Article