Premium
EP04.14: Utility of whole‐exome sequencing for genetic diagnosis of continuous fetuses with similar sonographic abnormalities in two pedigrees
Author(s) -
L. Benitez Quintanilla,
Célia Bádenas,
Victoria López,
V. Borobio,
M. Pauta,
A. Borrell
Publication year - 2019
Publication title -
ultrasound in obstetrics and gynecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.202
H-Index - 141
eISSN - 1469-0705
pISSN - 0960-7692
DOI - 10.1002/uog.21169
Subject(s) - pedigree chart , medicine , exome sequencing , genetic diagnosis , fetus , prenatal diagnosis , computational biology , exome , genetics , obstetrics , mutation , pregnancy , gene , biology
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom