Deletion 9q34.3 syndrome: Genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

S. A. Yatsenko, S. W. Cheung, D. A. Scott, M. J.M. Nowaczyk, M. Tarnopolsky, S. Naidu, G. Bibat, A. Patel, J. G. Leroy, F. Scaglia, P. Stankiewicz, James R. Lupski

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