Molecular cytogenetic characterization of 1q42.3q44 deletion and 8q24.3 duplication in a fetus with single umbilical artery and ventricular septal defects

Author:

Yue Fagui,Sun Meiling,Zhang Hongguo,Jiang Yuting,Li Leilei,He Jing,Liu Ruizhi

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference26 articles.

1. Terminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old female;Mankinen;Birth Defects Orig Artic Ser,1976

2. Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation;Mohamed;Mol Cytogenet,2018

3. Two new cases of pure 1q terminal deletion presenting with brain malformations;Hiraki;Am J Med Genet,2008

4. A 46,XY female with a 9p24.3p24.1 deletion and a 8q24.11q24.3 duplication: a case report and review of the literature;Bruni;Cytogenet Genome Res,2019

5. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype;Concolino;Eur J Med Genet,2012

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