Prenatal diagnosis of monosomy 18p associated with holoprosencephaly: case report-Reference-Cited by-同舟云学术

Prenatal diagnosis of monosomy 18p associated with holoprosencephaly: case report

Published:2017-05-17 Issue:6 Volume:37 Page:804-806
ISSN:0144-3615
Container-title:Journal of Obstetrics and Gynaecology
language:en
Short-container-title:Journal of Obstetrics and Gynaecology

Author:

Yin Zhaochu¹²,Zhang Kai³,Ni Bin²,Fan Xiongwei¹,Wu Xiushan¹

Affiliation:

1. The Center for Heart Development, State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Sciences, Hunan Normal University, Changsha, Hunanm, P.R. China;

2. Birth Health & Genetics Lab, Parenthood research institute of Hunan Province, Changsha, Hunan Province, P.R. China;

3. Department of geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China

Funder

department of science and technology

Hunan province, China and National Natural Science Foundation of China

Hunan Provincial NaturalScience Foundation of China

Cooperative Innovation Center of Engineering and New Products for Developmental Biology of Hunan Province

Scientific Research Fund of Hunan Provincial Education Department

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology

Link

https://www.tandfonline.com/doi/pdf/10.1080/01443615.2017.1306836

Reference9 articles.

1. Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation

2. A primary cilia-dependent etiology for midline facial disorders

3. Prenatal Diagnosis of Alobar Holoprosencephaly, Cyclopia, Proboscis, and Isochromosome 18q in the Second Trimester

4. Cyclopia: a radiological and anatomical craniofacial post mortem study

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