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  • Erratum
  • Open Access

Erratum to: Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome

  • 1,
  • 2,
  • 1,
  • 2,
  • 3,
  • 2,
  • 3,
  • 4,
  • 1,
  • 5,
  • 6,
  • 7 and
  • 8Email author
BMC GeneticsBMC series – open, inclusive and trusted201718:9

https://doi.org/10.1186/s12863-017-0480-z

  • Received: 24 January 2017
  • Accepted: 27 January 2017
  • Published:

The original article was published in BMC Genetics 2017 18:3

Erratum

Shortly after the publication of this article [1], one of the authors noticed that his name had been misspelled. The article has been updated. ‘Puthen Jitesh’ has been changed to ‘Puthen Jithesh’.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Unité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon
(2)
Bioinformatics Division, Sidra Medical & Research Center, Doha, Qatar
(3)
Genomics Core Laboratory, Translational Medicine Division, Sidra Medical & Research Center, Doha, Qatar
(4)
Research office, Sidra Medical & Research Center, Doha, Qatar
(5)
Department of Radiology, Hotel Dieu de France University hospital–Beirut, Beirut, Lebanon
(6)
Department of General surgery, Dar Al Amal University Hospital-Baalbeck, Baalbeck, Lebanon
(7)
Laboratory of Genetic Medicine and Immunology, Weill Cornell Medicine-Qatar, Doha, Qatar
(8)
Institut Jérôme Lejeune, 37, rue des Volontaires, Paris, 75015, France

References

  1. Zahraa H, Ramzi T, Eliane C, Puthen J, Wei L, Rashid A-A, Ena W, Marincola FM, Nadine J, Soha H, Wassim H, Lotfi C, André M. Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome. BMC Genet. 2017;18:3. doi:10.1186/s12863-017-0471-0.Google Scholar

Copyright

© The Author(s). 2017

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