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Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data

Published in 2023 by Erandee Robertson, Bronwyn E. Grinton, Karen L. Oliver ORCID, Liam G. Fearnley, Michael S. Hildebrand ORCID, Lynette G. Sadleir, Ingrid E. Scheffer, Samuel F. Berkovic, Mark F. Bennett, Melanie Bahlo
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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