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A de novo 2.2 Mb recurrent 17q23.1q23.2 deletion unmasks novel putative regulatory non-coding SNVs associated with lethal lung hypoplasia and pulmonary hypertension: a case report

Overview of attention for article published in BMC Medical Genomics, March 2020
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Title
A de novo 2.2 Mb recurrent 17q23.1q23.2 deletion unmasks novel putative regulatory non-coding SNVs associated with lethal lung hypoplasia and pulmonary hypertension: a case report
Published in
BMC Medical Genomics, March 2020
DOI 10.1186/s12920-020-0701-6
Pubmed ID
Authors

Justyna A. Karolak, Tomasz Gambin, Engela M. Honey, Tomas Slavik, Edwina Popek, Paweł Stankiewicz

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 19%
Student > Doctoral Student 3 11%
Student > Bachelor 2 7%
Professor > Associate Professor 2 7%
Student > Master 2 7%
Other 4 15%
Unknown 9 33%
Readers by discipline Count As %
Medicine and Dentistry 7 26%
Biochemistry, Genetics and Molecular Biology 5 19%
Nursing and Health Professions 1 4%
Sports and Recreations 1 4%
Agricultural and Biological Sciences 1 4%
Other 0 0%
Unknown 12 44%