Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2007/08/29
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Journal
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Indian UGC (journal)
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Refrences23
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Citations46
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S‐HL Kang
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A Scheffer
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Z Ou
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J Li
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F Scaglia
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J Belmont
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SR Lalani
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E Roeder
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V Enciso
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S Braddock
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J Buchholz
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S Vacha
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AC Chinault
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SW Cheung
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CA Bacino
Abstract
Cite
Kang, S‐HL, et al. “Identification of Proximal 1p36 Deletions Using array‐CGH: A Possible New Syndrome”. Clinical Genetics, vol. 72, no. 4, 2007, pp. 329-38, https://doi.org/10.1111/j.1399-0004.2007.00876.x.
Kang, S., Scheffer, A., Ou, Z., Li, J., Scaglia, F., Belmont, J., Lalani, S., Roeder, E., Enciso, V., Braddock, S., Buchholz, J., Vacha, S., Chinault, A., Cheung, S., & Bacino, C. (2007). Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome. Clinical Genetics, 72(4), 329-338. https://doi.org/10.1111/j.1399-0004.2007.00876.x
Kang S, Scheffer A, Ou Z, Li J, Scaglia F, Belmont J, et al. Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome. Clinical Genetics. 2007;72(4):329-38.
Journal Categories
Medicine
Medicine (General)
Medicine
Medicine (General)
Medical technology
Science
Biology (General)
Genetics
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Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| Monosomy 1p36 | Journal of Medical Genetics |
| 1999 | |
| Constitutional 1p36 deletion in a child with neuroblastoma | 1993 | |||
| Pure trisomy 17q from a 17;21 translocation | 1993 | |||
| CHD5 Is a Tumor Suppressor at Human 1p36 | Cell |
| 239 | 2007 |
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality | Clinical Genetics |
| 100 | 2003 |
Citations
Citations Analysis
The category
Science: Biology (General): Genetics 25
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Brain structure, function, and genetics revealed by studies of the eye and face and was published in 2008. The most recent citation comes from a 2023 study titled A Rare Case of an Infant With 1p36 Deletion Syndrome Presenting With Systolic Heart Failure Secondary to Severe Dilated Cardiomyopathy. This article reached its peak citation in 2018, with 6 citations. It has been cited in 34 different journals, 23% of which are open access. Among related journals, the American Journal of Medical Genetics Part A cited this research the most, with 8 citations. The chart below illustrates the annual citation trends for this article.