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Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome

Crossref DOI link: https://doi.org/10.1038/gim.2016.14

Published Print: 2016-11

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Weerakkody, Ruwan A. https://orcid.org/0000-0002-6717-7383
Vandrovcova, Jana https://orcid.org/0000-0002-3664-3724
Kanonidou, Christina

Mueller, Michael

Gampawar, Piyush

Ibrahim, Yousef https://orcid.org/0000-0001-9151-1241
Norsworthy, Penny https://orcid.org/0000-0002-5572-8491
Biggs, Jennifer

Abdullah, Abdulshakur

Ross, David https://orcid.org/0000-0002-6340-3742
Black, Holly A.

Ferguson, David

Cheshire, Nicholas J.

Kazkaz, Hanadi

Grahame, Rodney

Ghali, Neeti

Vandersteen, Anthony

Pope, F. Michael

Aitman, Timothy J.
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Text and Data Mining valid from 2016-11-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2016.14

Content Type: article

Copyright: © 2016, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics