Mosaic trisomy 9 presenting with congenital heart disease, facial dysmorphism and pigmentary skin lesions: Intricate issues of genetic counseling
Indian Journal of Pediatrics, ISSN: 0019-5456, Vol: 79, Issue: 6, Page: 806-809
2012
- 7Citations
- 15Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations7
- Citation Indexes7
- CrossRef2
- Captures15
- Readers15
- 15
Article Description
Chromosomal mosaicism for full aneuploidy involving chromosome 9 is an uncommon chromosomal abnormality. Mosaic trisomy 9 clinical manifestations are highly variable and difficult to predict. The authors present a case of mosaic trisomy 9 with typical clinical manifestations (facial dysmorphism, various internal organ malformations and severe psychomotor retardation), pigmentary mosaic skin lesions along the lines of Blaschko and evidence of maternal uniparental disomy in skin.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84864264373&origin=inward; http://dx.doi.org/10.1007/s12098-011-0567-x; http://www.ncbi.nlm.nih.gov/pubmed/21975655; http://link.springer.com/10.1007/s12098-011-0567-x; https://dx.doi.org/10.1007/s12098-011-0567-x; https://link.springer.com/article/10.1007/s12098-011-0567-x; http://www.springerlink.com/index/10.1007/s12098-011-0567-x; http://www.springerlink.com/index/pdf/10.1007/s12098-011-0567-x
Springer Science and Business Media LLC
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