Kortschak RD، Reimann H، Zimmer M، Eyre HJ، Saint R، Jenne DE (يوليو 1998). "The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome". Genomics. ج. 51 ع. 2: 288–92. DOI:10.1006/geno.1998.5259. PMID:9722953.
Kortschak RD، Reimann H، Zimmer M، Eyre HJ، Saint R، Jenne DE (يوليو 1998). "The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome". Genomics. ج. 51 ع. 2: 288–92. DOI:10.1006/geno.1998.5259. PMID:9722953.