APA

Coci E. G., Koehler U., Liehr T., Stelzner A., Fink C., Langen H. & Riedel J. (20160205). CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes. : Molecular cytogenetics.

Chicago

Coci Emanuele G, Koehler Udo, Liehr Thomas, Stelzner Armin, Fink Christian, Langen Hendrik and Riedel Joachim. 20160205. CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes. : Molecular cytogenetics.

Harvard

Coci E. G., Koehler U., Liehr T., Stelzner A., Fink C., Langen H. and Riedel J. (20160205). CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes. : Molecular cytogenetics.

MLA

Coci Emanuele G, Koehler Udo, Liehr Thomas, Stelzner Armin, Fink Christian, Langen Hendrik and Riedel Joachim. CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes. : Molecular cytogenetics. 20160205.