A comprehensive global genotype–phenotype database for rare diseases

Molecular Genetics and Genomic Medicine

Volumn 5, Issue 1, 2017, Pages 66-75

  Trujillano, Daniel ^a   Oprea, Gabriela Elena ^a   Schmitz, Yvonne ^a   Bertoli Avella, Aida M ^a   Abou Jamra, Rami ^a,b   Rolfs, Arndt ^a,c  

^a CENTOGENE AG   (Germany)

^b UNIVERSITY OF LEIPZIG   (Germany)

^c UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

Clinical diagnostics; HPO; rare disease; variant database

Indexed keywords

EID: 85032380172     PISSN: None     EISSN: 23249269     Source Type: Journal    
DOI: 10.1002/mgg3.262     Document Type: Article

References (22)

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