Kleefstra, T., Brunner, H. G., Amiel, J., Oudakker, A. R., Nillesen, W. M., Magee, A., . . . van Bokhoven, H. (2006). Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome. The American Society of Human Genetics.
Chicago Style CitationKleefstra, Tjitske, et al. Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome. The American Society of Human Genetics, 2006.
Cita MLAKleefstra, Tjitske, et al. Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome. The American Society of Human Genetics, 2006.
Atenció: Aquestes cites poden no estar 100% correctes.