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Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants

Overview of attention for article published in BMC Medical Genomics, June 2020
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Title
Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
Published in
BMC Medical Genomics, June 2020
DOI 10.1186/s12920-020-00737-6
Pubmed ID
Authors

Joakim Klar, Helene Engstrand-Lilja, Khurram Maqbool, Jonas Mattisson, Lars Feuk, Niklas Dahl

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 5 36%
Student > Ph. D. Student 2 14%
Student > Master 2 14%
Professor 1 7%
Other 1 7%
Other 1 7%
Unknown 2 14%
Readers by discipline Count As %
Unspecified 5 36%
Medicine and Dentistry 4 29%
Biochemistry, Genetics and Molecular Biology 2 14%
Nursing and Health Professions 1 7%
Unknown 2 14%