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A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics

Overview of attention for article published in Molecular Cytogenetics, April 2014
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Title
A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics
Published in
Molecular Cytogenetics, April 2014
DOI 10.1186/1755-8166-7-26
Pubmed ID
Authors

Aihua Yin, Jian Lu, Chang Liu, Li Guo, Jing Wu, Mingqin Mai, Yanfang Zhong, Xiaozhuang Zhang

Abstract

Array-based comparative genomic hybridization possesses a number of significant advantages over conventional cytogenetic and other molecular cytogenetic techniques, providing a sensitive and comprehensive detection platform for unexpected imbalances in the genome wide.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 1 4%
Unknown 22 96%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 8 35%
Researcher 4 17%
Student > Ph. D. Student 4 17%
Student > Doctoral Student 2 9%
Other 1 4%
Other 0 0%
Unknown 4 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 6 26%
Medicine and Dentistry 5 22%
Biochemistry, Genetics and Molecular Biology 3 13%
Business, Management and Accounting 1 4%
Nursing and Health Professions 1 4%
Other 3 13%
Unknown 4 17%