Periconceptional folic acid intake and disturbing factors: A single-center study in Japan [0.03%]
孕早期叶酸摄入及影响因素：日本单中心研究
Shunsuke Kamura,Aiko Sasaki,Kohei Ogawa et al.
Shunsuke Kamura et al.
We investigated folic acid (FA) intake and disturbing factors in pregnant women who visited our center in 2017. Among 1531 pregnant women, 45.1% of women initiated FA supplementation before pregnancy. The risk of failure of supplementation ...
Retracted: A preliminary study on the quantification of soft palate movement using ultrasonography [0.03%]
软腭运动的超声定量研究初步报告 [已撤稿]
Retraction: [Kumiko Fujiwara, Satoru Saitou, Naomi Nakamichi, Kei Tomihara, Hideyuki Hasegawa and Makoto Noguchi, A preliminary study on the quantification of soft palate movement using ultrasonography, Congenital Anomalies, in Early View: ...
Retraction of Publication
Congenital anomalies. 2023 May;63(3):90. DOI:10.1111/cga.12446 2023
A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings [0.03%]
日本一家出现杂合子刺猬基因新型突变表现出广泛的临床和放射学特征的家庭研究
Takanori Onuki,Nao Shibata,Shota Hiroshima et al.
Takanori Onuki et al.
Changes in the birth prevalence of orofacial clefts in Japan: Has the birth prevalence of orofacial clefts been affected by improved accuracy of prenatal diagnosis? [0.03%]
日本唇腭裂出生患病率的变化：产前诊断准确性的提高是否影响了唇腭裂的出生患病率？
Nagato Natsume,Hiroo Furukawa,Teruyuki Niimi et al.
Nagato Natsume et al.
We have been conducting a survey on the birth prevalence of orofacial clefts, including cleft lip with or without cleft palate and cleft palate, in the Tokai area in central Japan every year for 37 years. Along with the yearly trends in the...
The association between the congenital heart diseases and congenital anomalies of the kidney and the urinary tract in nonsyndromic children [0.03%]
非综合征儿童先天性心脏病与泌尿系统先天性畸形的相关性研究
Esma Keleş Alp,Muhammet İrfan Dönmez,Hayrullah Alp et al.
Esma Keleş Alp et al.
Several congenital heart diseases (CHD) are present in children with congenital anomalies of the kidney and the urinary tract (CAKUT) in syndromic or nonsyndromic patterns. The purpose of this study was to identify nonsyndromic children wit...
Parenchymal calcification is associated with the neurological prognosis in patients with congenital rubella syndrome [0.03%]
风疹先天性综合征患者神经预后与实质钙化有关
Takahiro Namiki,Chika Takano,Ryoji Aoki et al.
Takahiro Namiki et al.
Congenital rubella syndrome (CRS) results from maternal rubella virus infection in early pregnancy. Abnormal neuroimaging findings have been analyzed in a small number of CRS patients in the past; however, their clinical significance has be...
A rare congenital esophageal anomaly mimicking an isolated esophageal atresia: Kluth Type IV1a membranous esophageal atresia [0.03%]
一种罕见的先天性食管畸形，类似于孤立性食管闭锁：克卢特四型1a膜性食管闭锁
Ozlem Boybeyi-Turer,Irem Iyigun,Murat Cagan et al.
Ozlem Boybeyi-Turer et al.
Congenital esophageal web is a very rare type of esophageal atresia (EA) and is considered as Type IV atresia in Kluth's classification. Type IV EA is further classified into subgroups according to the location of web and the presence of tr...
Ahmed Eshiba,Samar Eshiba,Mostafa Kotb et al.
Ahmed Eshiba et al.
Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly [0.03%]
全外显子组测序在伴有中轴并骨症的伊朗家系中鉴定到BHLHA9新移码突变
Sahar Sadat Sedighzadeh,Alireza Sedaghat,Mina Zamani et al.
Sahar Sadat Sedighzadeh et al.
Mesoaxial synostotic syndactyly with phalangeal reduction (MSSD) represents a rare non-syndromic defect with an autosomal recessive pattern of inheritance. Sequence variants in the BHLHA9 gene cause MSSD and to date only a few mutations in ...
Stage-dependent function of Wnt5a during male external genitalia development [0.03%]
Wnt5a在性别决定过程中的阶段特异性功能研究新进展——以男性外生殖器发育为例
Mellissa C Alcantara,Kentaro Suzuki,Alvin R Acebedo et al.
Mellissa C Alcantara et al.
External genitalia development in mice involves multiple developmental processes under the regulation of various signaling pathways. Wnt5a, one of the major Wnt ligands, is a crucial developmental regulator of outgrowing organs such as the ...