Filges, I., Kang, A., Klug, V., Wenzel, F., Heinimann, K., Tercanli, S., & Miny, P. (2012). Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies. BioMed Central.
Citação norma ChicagoFilges, Isabel, Anjeung Kang, Vanessa Klug, Friedel Wenzel, Karl Heinimann, Sevgi Tercanli, and Peter Miny. Array Comparative Genomic Hybridization in Prenatal Diagnosis of First Trimester Pregnancies At High Risk for Chromosomal Anomalies. BioMed Central, 2012.
MLA citiranjeFilges, Isabel, et al. Array Comparative Genomic Hybridization in Prenatal Diagnosis of First Trimester Pregnancies At High Risk for Chromosomal Anomalies. BioMed Central, 2012.
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