Identification of EPCAM mutation: clinical use of microarray.
Publication
, Journal Article
Tan, QK-G; Cardona, DM; Rehder, CW; McDonald, MT
Published in: Clin Case Rep
June 2017
We report a case of an infant with congenital tufting enteropathy (CTE) who presented with severe failure to thrive despite multiple interventions. This study illustrates that CTE may be missed by endoscopy, and the use of chromosomal microarray and immunohistological analysis may be integral to diagnosis.
Duke Scholars
Published In
Clin Case Rep
DOI
ISSN
2050-0904
Publication Date
June 2017
Volume
5
Issue
6
Start / End Page
980 / 985
Location
England
Related Subject Headings
- 42 Health sciences
- 32 Biomedical and clinical sciences
- 30 Agricultural, veterinary and food sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Tan, Q.-G., Cardona, D. M., Rehder, C. W., & McDonald, M. T. (2017). Identification of EPCAM mutation: clinical use of microarray. Clin Case Rep, 5(6), 980–985. https://doi.org/10.1002/ccr3.914
Tan, Queenie K-G, Diana M. Cardona, Catherine W. Rehder, and Marie T. McDonald. “Identification of EPCAM mutation: clinical use of microarray.” Clin Case Rep 5, no. 6 (June 2017): 980–85. https://doi.org/10.1002/ccr3.914.
Tan QK-G, Cardona DM, Rehder CW, McDonald MT. Identification of EPCAM mutation: clinical use of microarray. Clin Case Rep. 2017 Jun;5(6):980–5.
Tan, Queenie K. G., et al. “Identification of EPCAM mutation: clinical use of microarray.” Clin Case Rep, vol. 5, no. 6, June 2017, pp. 980–85. Pubmed, doi:10.1002/ccr3.914.
Tan QK-G, Cardona DM, Rehder CW, McDonald MT. Identification of EPCAM mutation: clinical use of microarray. Clin Case Rep. 2017 Jun;5(6):980–985.
Published In
Clin Case Rep
DOI
ISSN
2050-0904
Publication Date
June 2017
Volume
5
Issue
6
Start / End Page
980 / 985
Location
England
Related Subject Headings
- 42 Health sciences
- 32 Biomedical and clinical sciences
- 30 Agricultural, veterinary and food sciences