The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.
- DOI
- 10.1002/ajmg.c.31662
- Published
- 2018 Dec
- Container
- American journal of medical genetics. Part C, Seminars in medical genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/ajmg.c.31662,
title = {The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.},
author = {Hartley T and Balcı TB and Rojas SK and Eaton A and Canada CR and Dyment DA and Boycott KM},
year = {2018},
journal = {American journal of medical genetics. Part C, Seminars in medical genetics},
doi = {10.1002/ajmg.c.31662},
url = {https://doi.org/10.1002/ajmg.c.31662}
}RIS
TY - JOUR TI - The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®. AU - Hartley T AU - Balcı TB AU - Rojas SK AU - Eaton A AU - Canada CR AU - Dyment DA AU - Boycott KM PY - 2018 JO - American journal of medical genetics. Part C, Seminars in medical genetics DO - 10.1002/ajmg.c.31662 UR - https://doi.org/10.1002/ajmg.c.31662 ER -
APA
T, H., TB, B., SK, R., A, E., CR, C., DA, D., & KM, B. (2018). The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.. American journal of medical genetics. Part C, Seminars in medical genetics. https://doi.org/10.1002/ajmg.c.31662
Source records
- pubmed · retrieved 2026-09-25T16:28:18.890Z