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Paper Details

Application of full-genome analysis to diagnose rare monogenic disorders.
NPJ Genom Med
21
2021
genomes, monogenic, monogenic disorders, non-coding duplication, rare diseases
Author NameAffiliation
Anne SlavotinekInstitute for Human Genetics, University of California San Francisco
Anne SlavotinekBenioff Children's Hospital, University of California San Francisco
Anne SlavotinekInstitute for Human Genetics, University of California San Francisco
Anne SlavotinekBenioff Children's Hospital, University of California San Francisco
Steven E BrennerUniversity of California Berkeley
Steven E BrennerUniversity of California Berkeley
Pui-Yan KwokInstitute for Human Genetics, University of California San Francisco
Pui-Yan KwokCardiovascular Research Institute, University of California San Francisco
Pui-Yan KwokUniversity of California San Francisco
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