Cite

Overlapping phenotypes between <scp>SHORT</scp> and Noonan syndromes in patients with <scp> PTPN11 </scp> pathogenic variants

MLA

Charles Marques, et al. “Overlapping Phenotypes between SHORT and Noonan Syndromes in Patients with PTPN11 Pathogenic Variants.” Clinical Genetics, vol. 98, Apr. 2020, pp. 10–18. EBSCOhost, https://doi.org/10.1111/cge.13746.



APA

Charles Marques, Yline Capri, Anne Guimier, A. Micheil Innes, Jeanne Amiel, Martine Auclair, Julien Thevenon, David A. Dyment, Gilles Morin, Christel Thauvin-Robinet, Corinne Vigouroux, Emmanuelle Ranza, Michèle Mathieu-Dramard, Alain Verloes, & Laurence Faivre. (2020). Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants. Clinical Genetics, 98, 10–18. https://doi.org/10.1111/cge.13746



Chicago

Charles Marques, Yline Capri, Anne Guimier, A. Micheil Innes, Jeanne Amiel, Martine Auclair, Julien Thevenon, et al. 2020. “Overlapping Phenotypes between SHORT and Noonan Syndromes in Patients with PTPN11 Pathogenic Variants.” Clinical Genetics 98 (April): 10–18. doi:10.1111/cge.13746.