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HARVARD Citation
Wang, Q. et al. (2022). Deep phenotyping and whole‐exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders. Molecular genetics & genomic medicine. 10 (5), p. n/a. [Online].
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Wang, Q. et al. (2022). Deep phenotyping and whole‐exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders. Molecular genetics & genomic medicine. 10 (5), p. n/a. [Online].