Hersmus, R., Stoop, H., Turbitt, E., Oosterhuis, J. W., Drop, S. L., Sinclair, A. H., . . . Looijenga, L. H. (2012). SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype. BioMed Central.
Citação norma ChicagoHersmus, Remko, Hans Stoop, Erin Turbitt, J Wolter Oosterhuis, Stenvert LS Drop, Andrew H. Sinclair, Stefan J. White, and Leendert HJ Looijenga. SRY Mutation Analysis By Next Generation (deep) Sequencing in a Cohort of Chromosomal Disorders of Sex Development (DSD) Patients With a Mosaic Karyotype. BioMed Central, 2012.
MLA citiranjeHersmus, Remko, et al. SRY Mutation Analysis By Next Generation (deep) Sequencing in a Cohort of Chromosomal Disorders of Sex Development (DSD) Patients With a Mosaic Karyotype. BioMed Central, 2012.