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Volumn 45, Issue D1, 2017, Pages D865-D876

The human phenotype ontology in 2017

(59)  Köhler, Sebastian a   Vasilevsky, Nicole A b   Engelstad, Mark b   Foster, Erin b   McMurry, Julie b   Aymé, Ségolène c   Baynam, Gareth d,e   Bello, Susan M f   Boerkoel, Cornelius F g   Boycott, Kym M h   Brudno, Michael i,y   Buske, Orion J i,y   Chinnery, Patrick F j,k   Cipriani, Valentina l,m   Connell, Laureen E n   Dawkins, Hugh J S o   DeMare, Laura E n   Devereau, Andrew D p   De Vries, Bert B A q   Firth, Helen V r   more..


Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; DISEASE REGISTRY; GENE IDENTIFICATION; GENOMICS; HUMAN; HUMAN PHENOTYPE ONTOLOGY; ONTOLOGY; PERSONALIZED MEDICINE; PHENOTYPE; RARE DISEASE; SOFTWARE; TRANSLATIONAL RESEARCH; WHOLE EXOME SEQUENCING; BIOLOGICAL ONTOLOGY; BIOLOGY; GENETIC ASSOCIATION STUDY; PROCEDURES; RARE DISEASES;

EID: 85015982066     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkw1039     Document Type: Article
Times cited : (622)

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