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17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2018
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Citations

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Title
17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype
Published in
Orphanet Journal of Rare Diseases, July 2018
DOI 10.1186/s13023-018-0838-y
Pubmed ID
Authors

Yuqi Shen, Nuo Si, Zhe Liu, Fang Liu, Xiaolu Meng, Ying Zhang, Xue Zhang

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 23%
Student > Master 2 15%
Unspecified 1 8%
Student > Bachelor 1 8%
Student > Doctoral Student 1 8%
Other 2 15%
Unknown 3 23%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 46%
Medicine and Dentistry 2 15%
Social Sciences 1 8%
Unspecified 1 8%
Unknown 3 23%