Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies.

MLA

Monzani, Alice, et al. “Co-Occurrence of Genomic Imbalances on Xp22.1 in the SHOX Region and 15q25.2 in a Girl with Short Stature, Precocious Puberty, Urogenital Malformations and Bone Anomalies.” BMC Medical Genomics, vol. 12, no. 1, Jan. 2019, p. 5. EBSCOhost, https://doi.org/10.1186/s12920-018-0445-8.

APA

Monzani, A., Babu, D., Mellone, S., Genoni, G., Fanelli, A., Prodam, F., Bellone, S., & Giordano, M. (2019). Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies. BMC Medical Genomics, 12(1), 5. https://doi.org/10.1186/s12920-018-0445-8

Chicago

Monzani, Alice, Deepak Babu, Simona Mellone, Giulia Genoni, Antonella Fanelli, Flavia Prodam, Simonetta Bellone, and Mara Giordano. 2019. “Co-Occurrence of Genomic Imbalances on Xp22.1 in the SHOX Region and 15q25.2 in a Girl with Short Stature, Precocious Puberty, Urogenital Malformations and Bone Anomalies.” BMC Medical Genomics 12 (1): 5. doi:10.1186/s12920-018-0445-8.