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Yokoyama E, Smith-Pellegrin DL, Sánchez S, et al. 7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype. Mol Cytogenet. 2017;10:42doi: 10.1186/s13039-017-0345-1.
Yokoyama, E., Smith-Pellegrin, D. L., Sánchez, S., Molina, B., Rodríguez, A., Juárez, R., Lieberman, E., Avila, S., Castrillo, J. L., Del Castillo, V., & Frías, S. (2017). 7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype. Molecular cytogenetics, 1042. https://doi.org/10.1186/s13039-017-0345-1
Yokoyama, Emiy, et al. "7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype." Molecular cytogenetics vol. 10 (2017): 42. doi: https://doi.org/10.1186/s13039-017-0345-1
Yokoyama E, Smith-Pellegrin DL, Sánchez S, Molina B, Rodríguez A, Juárez R, Lieberman E, Avila S, Castrillo JL, Del Castillo V, Frías S. 7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype. Mol Cytogenet. 2017 Nov 15;10:42. doi: 10.1186/s13039-017-0345-1. eCollection 2017. PMID: 29177010; PMCID: PMC5688765.
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