The Indian Journal of Pediatrics

, Volume 84, Issue 11, pp 883–886 | Cite as

Clinical Features in Patients with Microdeletion at 6q14.1-q15

  • Qing Zhou
  • Xiao-Hui Wu
  • Yi-Can Yang
  • Chao-Chun Zou
Scientific Letter
  • 65 Downloads

Notes

Compliance with Ethical Standards

Conflict of Interest

None.

Source of Funding

This work is supported by Zhejiang Provincial Natural Science Foundation of China (LR13H090002), and the National Natural Science Foundation (81170787 & 81371215), and Zhejiang Provincial Program for the Cultivation of High-Level Innovative Health Talents (2014).

References

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    Zherebtsov MM, Klein RT, Aviv H, Toruner GA, Hanna NN, Brooks SS. Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature. Clin Dysmorphol. 2007;16:135–40.CrossRefPubMedGoogle Scholar
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    Hopkin RJ, Schorry E, Bofinger M, et al. New insights into the phenotypes of 6q deletions. Am J Med Genet. 1997;70:377–86.CrossRefPubMedGoogle Scholar
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    Klauck SM. Genetics of autism spectrum disorder. Eur J Hum Genet. 2006;14:714–20.CrossRefPubMedGoogle Scholar
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    Sebat J, Lakshmi B, Malhotra D, et al. Strong association of de novo copy number mutations with autism. Science. 2007;316:445–9.CrossRefPubMedPubMedCentralGoogle Scholar

Copyright information

© Dr. K C Chaudhuri Foundation 2017

Authors and Affiliations

  • Qing Zhou
    • 1
  • Xiao-Hui Wu
    • 1
  • Yi-Can Yang
    • 1
  • Chao-Chun Zou
    • 1
  1. 1.Department of Endocrinology, Children’s HospitalZhejiang University School of MedicineHangzhouChina

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