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Fetal Costello syndrome: description of phenotype of HRAS exon 1 mutations
Author(s) -
Schøler Nørgaard M.,
Mogra R.,
Pinner J.,
Kagan K. O.,
Warming Jørgensen M.,
Gjørup V.,
Petersen O. B.,
Sandager P.,
Vogel I.
Publication year - 2020
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.20281
Subject(s) - medicine , hras , prenatal diagnosis , nuchal translucency measurement , fetus , pregnancy , obstetrics , in utero , conjoined twins , colorectal cancer , cancer , biology , kras , genetics
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