Strom, S. P., Lozano, R., Lee, H., Dorrani, N., Mann, J., O’Lague, P. F., . . . Quintero-Rivera, F. (2014). De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing. BioMed Central.
Παραπομπή Chicago StyleStrom, Samuel P., et al. De Novo Variants in the KMT2A (MLL) Gene Causing Atypical Wiedemann-Steiner Syndrome in Two Unrelated Individuals Identified By Clinical Exome Sequencing. BioMed Central, 2014.
Παραπομπή MLAStrom, Samuel P., et al. De Novo Variants in the KMT2A (MLL) Gene Causing Atypical Wiedemann-Steiner Syndrome in Two Unrelated Individuals Identified By Clinical Exome Sequencing. BioMed Central, 2014.
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