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of 2
pro vyhledávání: '"Jesna Manoj"'
Autor:
Salah Basheer, Akhilesh Pandey, Satish Chandra Girimaji, Deepshikha Chandel, Somasekar Seshagiri, Babylakshmi Muthusamy, Srimonta Gayen, Lakshmi Dhevi N. Selvan, Thong T. Nguyen, Aravind K. Bandari, Jesna Manoj
Say-Meyer syndrome is a rare and clinically heterogeneous syndrome characterized by trigonocephaly, short stature, developmental delay and hypotelorism. Nine patients with this syndrome have been reported thus far although no causative gene has yet b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f833c2e49690ece9e1a0922eb4a73d
https://europepmc.org/articles/PMC6974397/
https://europepmc.org/articles/PMC6974397/
Autor:
K. S. S. Reddy, Sakthivel Murugan, Satish Chandra Girimaji, Weiru Wang, Thong T. Nguyen, Bijay S. Jaiswal, Babylakshmi Muthusamy, Vedam Laxmi Ramprasad, Lakshmi Dhevi N. Selvan, T. S. Keshava Prasad, Somasekar Seshagiri, Remya Raja, Harsha Gowda, Akhilesh Pandey, Jayarama S. Kadandale, Andrew S. Peterson, Ravi Gupta, Eric Stawiski, Jesna Manoj
Publikováno v:
Omics : a journal of integrative biology. 21(5)
Robust diagnostics for many human genetic disorders are much needed in the pursuit of global personalized medicine. Next-generation sequencing now offers new promise for biomarker and diagnostic discovery, in developed as well as resource-limited cou