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VP25.09: A novel compound heterozygous mutation in STIL gene identified in a Chinese family with presentation of fetal microcephaly
Author(s) -
Cheng C.,
Yang Y.,
Zhu X.,
Zhang T.,
Yang F.,
Chen F.,
Chen X.,
Zhao S.,
Guo J.
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.22720
Subject(s) - microcephaly , medicine , prenatal diagnosis , fetus , holoprosencephaly , sanger sequencing , pathology , anatomy , genetics , mutation , pregnancy , gene , biology , pediatrics