Whole exome sequencing identifies a novel FRAS1 mutation and aids in vitro fertilization with preimplantation genetic diagnosis in Fraser syndrome
Journal
Taiwanese journal of obstetrics & gynecology
Journal Volume
61
Journal Issue
3
Date Issued
2022-05
Author(s)
Abstract
To demonstrate the picture of a woman who had three times of pregnancies but fetuses were complicated with Fraser syndrome, a rare genetic disorder with multiple congenital anomalies.
Subjects
Fraser syndrome/genetics; Intrafamilial variance; Oligohydramnios; Prenatal diagnosis; Whole exome sequencing
SDGs