Literature DB >> 34000720

Prenatal Diagnosis of Snijders Blok-Campeau Syndrome in a Fetus with Macrocephaly.

Gustavo Malinger1, Chen Hoffmann2, Reuven Achiron3, Michal Berkenstadt4.   

Abstract

We present the prenatal imaging and whole exomics sequencing with the newly described Snijders Blok-Campeau macrocephaly syndrome.
© 2021 S. Karger AG, Basel.

Entities:  

Keywords:  Fetal brain; MRI; Macrocephaly; Snijders Blok-Campeau syndrome; Ultrasound; Whole-exome sequencing

Year:  2021        PMID: 34000720     DOI: 10.1159/000514326

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  1 in total

1.  Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report.

Authors:  Xi-Yong Fan
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2021 Sept 15
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.