Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly. Issue 4 (1st April 2005) - Yatsenko, S A; Cheung, S W; Scott, D A; Nowaczyk, M J M; Tarnopolsky, M; Naidu, S; Bibat, G; Patel, A; Leroy, J G; Scaglia, F; Stankiewicz, P; Lupski, J R