| Autor: |
Sanna-Cherchi, Simone, Kiryluk, Krzysztof, Burgess, Katelyn E., Bodria, Monica, Sampson, Matthew G., Hadley, Dexter, Nees, Shannon N., Sterken, Roel, Verbitsky, Miguel, Lozanovski, Vladimir J., Materna-Kiryluk, Anna, Perry, Brittany J., Carrea, Alba, Murtas, Corrado, Ristoska-Bojkovska, Nadica, Zaniew, Marcin, Flogelova, Hana, Weng, Patricia L., Arapovic, Adela, Drnasin, Kristina, Gianluca Caridi, Goj, Vinicio, Lifton, Richard P., Saraga, Marijan, Dominiczak, Anna F., Gesualdo, Loreto, Gucev, Zoran, Allegri, Landino, Latos-Bielenska, Anna, Cusi, Daniele, Scolari, Francesco, Tasic, Velibor, Hakonarson, Hakon, Ghiggeri, Gian Marco, Gharavi, Ali G. |
| Předmět: |
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| Zdroj: |
Publons
ResearcherID
Web of Science |
| Popis: |
Up to 16.6 % of patients with congenital kidney defects have a molecular diagnosis attributable to a genomic disorder. A search for genomic structural variantsis indicated in this patient population to diagnose theirspecific genomic disorders, conduct adequate geneticcounseling, and individualize medical care. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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