文献
J-GLOBAL ID:202002254659391189
整理番号:20A0536721
Robinow症候群の胎児におけるROR2遺伝子の全エクソーム配列決定複合ヘテロ接合変異体【JST・京大機械翻訳】
Whole-exome sequencing identified compound heterozygous variants in ROR2 gene in a fetus with Robinow syndrome
著者 (8件):
Yang Kai
(Department of Obstetrics and Gynecology, Peking University International Hospital, Beijing, China)
,
Zhu Jianjiang
(Department of Prenatal Diagnosis Center, Haidian Maternal and Child Health Care Hospital, Beijing, China)
,
Tan Ya
(Department of Obstetrics and Gynecology, Peking University International Hospital, Beijing, China)
,
Sun Xiaofei
(Department of Prenatal Diagnosis Center, Haidian Maternal and Child Health Care Hospital, Beijing, China)
,
Zhao Huawei
(Department of Prenatal Diagnosis Center, Haidian Maternal and Child Health Care Hospital, Beijing, China)
,
Tang Guodong
(Department of Prenatal Diagnosis Center, Haidian Maternal and Child Health Care Hospital, Beijing, China)
,
Zhang Dongliang
(Department of Orthodontics, School of Stomatology, Capital Medical University, Beijing, China)
,
Qi Hong
(Department of Prenatal Diagnosis Center, Haidian Maternal and Child Health Care Hospital, Beijing, China)
資料名:
Journal of Clinical Laboratory Analysis
(Journal of Clinical Laboratory Analysis)
巻:
34
号:
2
ページ:
e23074
発行年:
2020年
JST資料番号:
W2635A
ISSN:
0887-8013
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
アメリカ合衆国 (USA)
言語:
英語 (EN)