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The combination of whole‐exome sequencing and copy number variation sequencing enables the diagnosis of rare neurological disorders
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Journal Title: | Clinical Genetics |
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Authors and Corporations: | , , , , , , , |
In: | Clinical Genetics, 96, 2019, 2, p. 140-150 |
Type of Resource: | E-Article |
Language: | English |
published: |
Wiley
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Subjects: |