Prenatal diagnosis and molecular cytogenetic characterisation of hereditary chromosomal deletions with a favourable outcome-Reference-Cited by-同舟云学术

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Prenatal diagnosis and molecular cytogenetic characterisation of hereditary chromosomal deletions with a favourable outcome

Published:2019-04-25 Issue:6 Volume:39 Page:880-881
ISSN:0144-3615
Container-title:Journal of Obstetrics and Gynaecology
language:en
Short-container-title:Journal of Obstetrics and Gynaecology

Author:

Wang Bo¹,Yu Fei²,Xie Mingxia³,Sun Guoqiang⁴

Affiliation:

1. Department of Clinical Laboratory, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, PR China;

2. Department of Endocrine and Genetic Metabolism in Children, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, PR China;

3. Department of Obstetrics and Gynecology, The 457 Hospital of PLA, Wuhan, Hubei, PR China;

4. Department of Obstetrics, Maternal and Child Health Hospital of Hubei Province, Wuhan, Hubei, PR China

Funder

Hubei

P

provincial Health and Family Planning Commission

Publisher

Informa UK Limited

Subject

Obstetrics and Gynecology

Link

https://www.tandfonline.com/doi/pdf/10.1080/01443615.2019.1582617

Reference9 articles.

1. RORB gene and 9q21.13 microdeletion: Report on a patient with epilepsy and mild intellectual disability

2. Application of Array-Based Comparative Genomic Hybridization to Clinical Diagnostics

3. A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features

4. Increased expression of GCNT1 is associated with altered O -glycosylation of PSA, PAP, and MUC1 in human prostate cancers

5. Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature

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