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
Crossref DOI link: https://doi.org/10.1186/s13039-015-0163-2
Published Online: 2015-07-22
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Sheth, Frenny
Liehr, Thomas
Shah, Krati
Sheth, Jayesh
License valid from 2015-07-22