J Med Genet. 2005 April; 42(4): 328–335. | PMCID: PMC1736036 |
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
S Yatsenko, S Cheung, D Scott, M Nowaczyk, M Tarnopolsky, S Naidu, G Bibat, A Patel, J Leroy, F Scaglia, P Stankiewicz, and J Lupski
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