Literature DB >> 28513240

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

Zhaochu Yin1,2, Kai Zhang3, Bin Ni2, Xiongwei Fan1, Xiushan Wu1.   

Abstract

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Year:  2017        PMID： 28513240     DOI： 10.1080/01443615.2017.1306836

Source DB:  PubMed          Journal:  J Obstet Gynaecol        ISSN： 0144-3615            Impact factor:   1.246


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  3 in total

1.  The genotype and phenotype of chromosome 18p deletion syndrome: Case series.

Authors:  Qiujie Jin; Rong Qiang; Bo Cai; Xiaobin Wang; Na Cai; Shuai Zhen; Wen Zhai
Journal:  Medicine (Baltimore)       Date:  2021-05-07       Impact factor: 1.889

2.  Prenatal diagnosis of de novo monosomy 18p deletion syndrome by chromosome microarray analysis: Three case reports.

Authors:  Hong Qi; Jianjiang Zhu; Shaoqin Zhang; Lirong Cai; Xiaohui Wen; Wen Zeng; Guodong Tang; Yao Luo
Journal:  Medicine (Baltimore)       Date:  2019-04       Impact factor: 1.817

3.  A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing.

Authors:  Ganye Zhao; Peng Dai; Shanshan Gao; Xuechao Zhao; Conghui Wang; Lina Liu; Xiangdong Kong
Journal:  Mol Cytogenet       Date:  2019-12-21       Impact factor: 2.009
  3 in total

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