Literature DB >> 24456448

Prenatal diagnosis and molecular cytogenetic characterisation of a de novo 18p deletion.

G Fogu1, G Capobianco, F Cambosu, P Bandiera, A Pirino, M A Moro, P M Campus, G Soro, M Dessole, A Montella.   

Abstract

Mesh：

Year:  2014        PMID： 24456448     DOI： 10.3109/01443615.2013.834300

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


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  3 in total

1.  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

2.  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.  Familial microdeletion 18p11.32 to 18p11.31 in a Chinese family with normal phenotype.

Authors:  Miaomiao Han; Lei Wei; Fang Liu; Xia Gao
Journal:  Mol Cytogenet       Date:  2022-03-24       Impact factor: 2.009
  3 in total

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