The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®-Reference-Cited by-同舟云学术

The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®

Published:2018-12 Issue:4 Volume:178 Page:458-463
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Hartley Taila¹^ORCID,Balcı Tuğçe B.²^ORCID,Rojas Samantha K.¹,Eaton Alison¹^ORCID,Canada CareRare¹,Dyment David A.¹³^ORCID,Boycott Kym M.¹³^ORCID

Affiliation:

1. Children's Hospital of Eastern Ontario Research Institute, University of Ottawa; Ottawa Ontario Canada

2. Division of Genetics, Department of Pediatrics; London Health Sciences Centre; London Ontario Canada

3. Department of Genetics; Children's Hospital of Eastern Ontario; Ottawa Ontario Canada

Funder

Children's Hospital of Eastern Ontario Foundation

Ontario Research Fund

Genome Québec

Genome British Columbia

Genome Alberta

Canadian Institutes of Health Research

Ontario Genomics Institute

Genome Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference21 articles.

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