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المؤلفون: Mark A. Corbett, Gai L McMichael, C. L. van Eyk, Jozef Gecz, Alastair H. MacLennan, Dani L. Webber, Joshua A. Woenig, Kelly Harper, Morgan Newman, Jesia G. Berry, Bryan P. Haines, Mahalia S.B. Frank
المصدر: NPJ Genomic Medicine
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-11 (2019)مصطلحات موضوعية: 0301 basic medicine, Candidate gene, Genetic testing, lcsh:QH426-470, lcsh:Medicine, Biology, Article, Cerebral palsy, 03 medical and health sciences, 0302 clinical medicine, Neurodevelopmental disorder, Genetics, medicine, Clinical significance, Molecular Biology, Gene, Genetics (clinical), Disease burden, KIF1A, Molecular medicine, medicine.diagnostic_test, lcsh:R, Neurodevelopmental disorders, medicine.disease, Paediatric neurological disorders, lcsh:Genetics, 030104 developmental biology, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9fb3fb7289dab84380e9b39c3bcc6adTest
https://doi.org/10.1038/s41525-019-0101-zTest -
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المؤلفون: C. L. van Eyk, Alastair H. MacLennan, Mark A. Corbett
مصطلحات موضوعية: 0301 basic medicine, Heterogeneous group, business.industry, MEDLINE, Genetic variants, medicine.disease, Bioinformatics, Cerebral palsy, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Etiology, Medicine, Copy-number variation, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::f61e95454958ea060a830ec73f3a81c0Test
https://doi.org/10.1016/b978-0-444-63233-3.00022-1Test