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Novel FANCA mutation in the first fully-diagnosed patient with Fanconi anemia in Polish population – case report

Overview of attention for article published in Molecular Cytogenetics, August 2020
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Title
Novel FANCA mutation in the first fully-diagnosed patient with Fanconi anemia in Polish population – case report
Published in
Molecular Cytogenetics, August 2020
DOI 10.1186/s13039-020-00503-4
Pubmed ID
Authors

Anna Repczynska, Agata Pastorczak, Katarzyna Babol-Pokora, Jolanta Skalska-Sadowska, Malgorzata Drozniewska, Wojciech Mlynarski, Olga Haus

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 %
Student > Bachelor 2 14%
Student > Postgraduate 2 14%
Researcher 2 14%
Student > Ph. D. Student 1 7%
Unknown 7 50%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 36%
Chemical Engineering 1 7%
Computer Science 1 7%
Unknown 7 50%