Show items per page
Elements: 2
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction Borel, Christelle; Cheung, Fanny; Stewart, Helen; Koolen, David A; ... Sharp, Andrew J 2012
add to browser selection
Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis 2008