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Identification of Microdeletion of 7q36.1-qter in Fetal Hemivertebrae with Scoliosis

Author

Listed:
  • Yingjun Xie
  • Xiaofang Sun

    (Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, China)

  • Wei Jian
  • Jingsi Chen
  • Dunjin Chen

    (Prenatal Diagnosis Department, The Third Affiliated Hospital of Guangzhou Medical University, China)

Abstract

The 7q36 microdeletion has been identified in patients with variant phenotypes including sacral agenesis, holoprosencephaly and intellectual disability ...

Suggested Citation

  • Yingjun Xie & Xiaofang Sun & Wei Jian & Jingsi Chen & Dunjin Chen, 2018. "Identification of Microdeletion of 7q36.1-qter in Fetal Hemivertebrae with Scoliosis," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 9(5), pages 7458-7462, October.
  • Handle: RePEc:abf:journl:v:9:y:2018:i:5:p:7458-7462
    DOI: 10.26717/BJSTR.2018.9.001876
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    References listed on IDEAS

    as
    1. Ni Huang & Insuk Lee & Edward M Marcotte & Matthew E Hurles, 2010. "Characterising and Predicting Haploinsufficiency in the Human Genome," PLOS Genetics, Public Library of Science, vol. 6(10), pages 1-11, October.
    Full references (including those not matched with items on IDEAS)

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    More about this item

    Keywords

    Biomedical Sciences; Biomedical Research; Technical Research; Monosomy; 7q36.1-qter; Microarray Analysis; Genotype-Phenotype Correlation; Prenatal Diagnosis; Hemivertebrae Deformity;
    All these keywords.

    JEL classification:

    • R00 - Urban, Rural, Regional, Real Estate, and Transportation Economics - - General - - - General
    • Z0 - Other Special Topics - - General

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