文献
J-GLOBAL ID:202202219189876367
整理番号:22A0772643
単一三次センターで確認された48例における22q11.2微小欠失症候群の出生前超音波検査および細胞遺伝学的/分子的所見【JST・京大機械翻訳】
Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center
著者 (10件):
Sarac Sivrikoz Tugba
(Division of Perinatology, Department of Obstetrics and Gynecology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
,
Basaran Seher
(Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
,
Basaran Seher
(PREMED, Center for Genetic Diagnosis and Research, Istanbul, Turkey)
,
Has Recep
(Division of Perinatology, Department of Obstetrics and Gynecology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
,
Karaman Birsen
(Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
,
Karaman Birsen
(Department of Pediatric Basic Science, Child Health Institute, Istanbul University, Istanbul, Turkey)
,
Kalelioglu Ibrahim Halil
(Division of Perinatology, Department of Obstetrics and Gynecology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
,
Kirgiz Melike
(PREMED, Center for Genetic Diagnosis and Research, Istanbul, Turkey)
,
Altunoglu Umut
(Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
,
Yuksel Atil
(Division of Perinatology, Department of Obstetrics and Gynecology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey)
資料名:
Archives of Gynecology and Obstetrics
(Archives of Gynecology and Obstetrics)
巻:
305
号:
2
ページ:
323-342
発行年:
2022年
JST資料番号:
W4056A
ISSN:
1432-0711
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
ドイツ (DEU)
言語:
英語 (EN)