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BMC Biology|July 15, 2016
Type IV collagen drives alveolar epithelial-endothelial association and the morphogenetic movements of septationMaria Loscertales, Fotini Nicolaou, Marion Jeanne, et al.
Scientific Reports|October 29, 2025
Improved genomic characterization of a clinically heterogeneous pediatric cohort with WGS vs. WESAwtum M Brashear, Anxhela G Gustafson, Andrew Quitadamo, et al.
Tumori|December 9, 2017
Reliability and validity assessment of administrative databases in measuring the quality of rectal cancer managementCarlo Corbellini, Bruno Andreoni, Luca Ansaloni, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutationsMauro Longoni, Silvia Moncini, Mariangela Cisternino, et al.
American Journal of Medical Genetics. Part A|August 7, 2018
Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillanceKelly L Jones, Erin A McNamara, Mauro Longoni, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2012
Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomesMeaghan K Russell, Mauro Longoni, Julie Wells, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDHSibel Kantarci, Kate G Ackerman, Meaghan K Russell, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2018
Systematic analysis of copy number variation associated with congenital diaphragmatic herniaQihui Zhu, Frances A High, Chengsheng Zhang, et al.
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