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Duba HC, Erdel M, Löffler J, et al. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome. J Med Genet. 1997;34(4):309-13doi: 10.1136/jmg.34.4.309.
Duba, H. C., Erdel, M., Löffler, J., Bereuther, L., Fischer, H., Utermann, B., & Utermann, G. (1997). Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome. Journal of medical genetics, 34(4), 309-13. https://doi.org/10.1136/jmg.34.4.309
Duba, H C, et al. "Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome." Journal of medical genetics vol. 34,4 (1997): 309-13. doi: https://doi.org/10.1136/jmg.34.4.309
Duba HC, Erdel M, Löffler J, Bereuther L, Fischer H, Utermann B, Utermann G. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome. J Med Genet. 1997 Apr;34(4):309-13. doi: 10.1136/jmg.34.4.309. PMID: 9138155; PMCID: PMC1050918.
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