Works matching IS 17558166 AND DT 2016 AND VI 9 AND IP 1

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes.

Published in:

Molecular Cytogenetics (17558166), 2016, v. 9, n. 1, p. 1, doi. 10.1186/s13039-016-0219-y

By:

• Coci, Emanuele G.;
• Koehler, Udo;
• Liehr, Thomas;
• Stelzner, Armin;
• Fink, Christian;
• Langen, Hendrik;
• Riedel, Joachim

Publication type:

Article