Clinical Report

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome†

  1. Ching-Fen Chang1,2,
  2. Ling-Hui Li1,
  3. Chung-Hsing Wang3,
  4. Fuu-Jen Tsai4,
  5. Tsai-Chuan Chen1,
  6. Jer-Yuarn Wu1,
  7. Yuan-Tsong Chen1,*,
  8. Anne Chun-Hui Tsai3,5,*

Article first published online: 20 AUG 2010

DOI: 10.1002/ajmg.a.33580

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 152A, Issue 9, pages 2365–2371, September 2010

Additional Information

How to Cite

Chang, C.-F., Li, L.-H., Wang, C.-H., Tsai, F.-J., Chen, T.-C., Wu, J.-Y., Chen, Y.-T. and Tsai, A. C.-H. (2010), Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome. Am. J. Med. Genet., 152A: 2365–2371. doi: 10.1002/ajmg.a.33580

Author Information

  1. 1

    Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan

  2. 2

    Institute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan

  3. 3

    Department of Pediatrics, China Medical University Hospital, Taichung, Taiwan

  4. 4

    Department of Medical Genetics, College of Chinese Medicine, China Medical University Hospital, Taichung, Taiwan

  5. 5

    Section of Clinical Genetics and Metabolism, The Children's Hospital, Denver, University of Colorado School of Medicine, Colorado

*Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.

  1. †

    How to cite this article: Chang C-F, Li L-H, Wang C-H, Tsai F-J, Chen T-C, Wu J-Y, Chen Y-T, Tsai A.C.-H. 2010. Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome. Am J Med Genet Part A 152A:2365–2371.

Publication History

  1. Issue published online: 20 AUG 2010
  2. Article first published online: 20 AUG 2010
  3. Manuscript Accepted: 22 MAY 2010
  4. Manuscript Received: 8 MAY 2009

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