L-NAME, a nitric oxide synthase inhibitor, increases the protein expression of both executioner and inhibitor of apoptosis in the placental bed of mid-to-late pregnant rats [0.03%]
Nitric氧化物合成酶抑制剂L-NAME增加中晚期妊娠大鼠蜕膜细胞执行者和抑制者凋亡蛋白的表达
Wataru Ishikawa,Shugo Kazama,Takehito Suzuki et al.
Wataru Ishikawa et al.
The involvement of nitric oxide (NO) signaling in apoptosis was examined in the placental bed of mid-to-late pregnant rats. Pregnant rats were treated with l-NAME, a nitric oxide synthase inhibitor, by subcutaneous infusion for 48 hours bef...
Germline mosaicism in a collagen VI-related myopathy family: A cause of autosomal recessive inheritance [0.03%]
胶原VI相关肌病家系的生殖系镶嵌现象：一种常染色体隐性遗传的原因
Gui-Lan Chen,Dong-Zhi Li
Gui-Lan Chen
Breast reconstruction via fat grafting for a patient with bilateral congenital amastia (Finlay-Marks syndrome) [0.03%]
脂肪移植用于双侧先天性无乳症(Finlay-Marks综合症)患者的乳房再造
Riri Ito,Yuhei Yamamoto,Taku Maeda et al.
Riri Ito et al.
Case Reports
Congenital anomalies. 2021 Jul;61(4):142-143. DOI:10.1111/cga.12416 2021
Clinical features of congenital complete vaginal atresia combined with cervical aplasia: A retrospective study of 19 patients and literature review [0.03%]
先天性完全阴道闭锁合并宫颈发育不全的临床特征回顾性分析及文献复习
Ling Mei,Heng Zhang,Yueyue Chen et al.
Ling Mei et al.
Congenital vaginal atresia is a rare congenital reproductive tract abnormality. To assess the clinical manifestations and feasibility of preserving uterus for congenital complete vaginal atresia with cervical aplasia, nineteen cases who und...
Mini-microform cleft lip with complete cleft alveolus and palate: A case report [0.03%]
小型牙片状唇裂伴全牙槽裂和腭裂的病例报告
Kumiko Fujiwara,Mitsuna Yoshida,Naomi Nakamichi et al.
Kumiko Fujiwara et al.
Cleft lip and cleft alveolus are caused by incomplete fusion of the frontonasal and maxillary prominences. However, milder forms of cleft lip are rarely accompanied by cleft alveolus. Here, we report a rare case of mini-microform cleft lip ...
Case Reports
Congenital anomalies. 2021 Jul;61(4):133-137. DOI:10.1111/cga.12415 2021
Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India [0.03%]
ANXTR2基因新变异导致的玻璃样纤维瘤病综合征：印度病例报告
Chakshu Chaudhry,Parminder Kaur,Priyanka Srivastava et al.
Chakshu Chaudhry et al.
Case Reports
Congenital anomalies. 2021 Jul;61(4):140-141. DOI:10.1111/cga.12414 2021
Prenatal ultrasonographic findings and fetal/neonatal outcomes of body stalk anomaly [0.03%]
体蒂异常的产前超声表现及胎儿/新生儿结局
Hiromi Nagase,Makiko Ohyama,Masafumi Yamamoto et al.
Hiromi Nagase et al.
We studied 27 cases that were post or prenatally diagnosed with body stalk anomaly (BSA) using medical records of prenatal ultrasound findings, pregnancy outcomes, and fetal/neonatal prognosis during 1992 to 2018. Termination of pregnancy w...
Unmasking a recessive allele by a deletion: Early prenatal diagnosis of Bardet-Biedl syndrome in a Chinese family [0.03%]
中国一家族Bardet-Biedl综合征的产前诊断及一新隐性突变基因的发现
Xiang-Yi Jing,Fan Jiang,Dong-Zhi Li
Xiang-Yi Jing
Congenital anomalies in breech presentation: A nationwide record linkage study [0.03%]
横位出生缺陷的全国记录关联研究
Georg Macharey,Mika Gissler,Anna Toijonen et al.
Georg Macharey et al.
Our study aimed to determine if congenital anomalies are associated with breech presentation at delivery. We conducted a nationwide, retrospective population-based record linkage study and analyzed all singleton births in Finland from 1996 ...
Case of feeding disorder due to lymphangioma of the tongue: Importance in developing countries [0.03%]
舌囊肿引起的喂养障碍一例及对发展中国家的意义
Hideto Imura,Nagato Natsume,Teruyuki Niimi et al.
Hideto Imura et al.
Case Reports
Congenital anomalies. 2021 May;61(3):105-107. DOI:10.1111/cga.12410 2021