Sheth, F., Liehr, T., Shah, K., & Sheth, J. (2015). Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation. Mol Cytogenet.
Stile di citazione ChicagoSheth, Frenny, Thomas Liehr, Krati Shah, e Jayesh Sheth. "Prader-Willi Syndrome - Type 1 Deletion, a Consequence of an Unbalanced Translocation of Chromosomes 13 and 15, Easily to Be Mixed Up With a Robertsonian Translocation." Mol Cytogenet 2015.
Citazione MLASheth, Frenny, Thomas Liehr, Krati Shah, e Jayesh Sheth. "Prader-Willi Syndrome - Type 1 Deletion, a Consequence of an Unbalanced Translocation of Chromosomes 13 and 15, Easily to Be Mixed Up With a Robertsonian Translocation." Mol Cytogenet 2015.