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期刊名:Congenital anomalies

缩写:CONGENIT ANOM

ISSN:0914-3505

e-ISSN:1741-4520

IF/分区:1.6/Q2

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共收录本刊相关文章索引633
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Meenakshi Veeramani,Neerujah Balachandren,Yong Hwa Hong et al. Meenakshi Veeramani et al.
Prior studies have explored the links between congenital anomalies and assisted reproduction techniques, among other factors. However, it remains unclear whether a particular technique harbors an inherent risk of major congenital anomalies,...
Munekazu Komada,Niina Kiriyama,Rei Sugiyama et al. Munekazu Komada et al.
During pregnancy, the maternal environment is critical for normal ontogeny and central nervous system development. Occasionally, prenatal exposure to environmental factors affects tissue architecture and functional development of the brain,...
Martin Kamau,Krishan Sarna,Symon Guthua et al. Martin Kamau et al.
Cleft lip and palate deformities substantially burden individuals and families, particularly in low-income communities. However, a comprehensive understanding of the patterns and distribution of these deformities in Kenya remains limited. T...
Kana Hiromoto,Takahiro Yamada,Mio Tsuchiya et al. Kana Hiromoto et al.
In Japan, a limited number of laboratories perform comprehensive genetic testing for rare diseases; this study investigated the attitudes of these laboratories toward the disclosure of secondary finding (SF). Following a preliminary survey,...
Bindey Kumar,Priyankar Singh,Alok Ranjan et al. Bindey Kumar et al.
The aim was to establish a specific and definite connection between non-syndromic orofacial cleft patients and associated congenital heart disease (CHD). Following PRISMA guidelines, selective databases were searched for data collection. St...
Rebecca Bruns,Khurram Liaqat,Abdul Nasir et al. Rebecca Bruns et al.
Angelman syndrome (AS, MIM #105830) is a neurodevelopmental disorder characterized by severe intellectual disability, profound developmental delay, movement or balance problems, an excessively cheerful disposition, and seizures. AS results ...
Xiaojin Luo,Weiqiang Liu,Liang Hu et al. Xiaojin Luo et al.
The phenotype of SCA patients are diversities, make prenatal counseling and parental decision-making following the prenatal diagnosis of SCA more complicated and challenging. NIPT has higher sensitivity and specificity in screening trisomy ...
Mariko Usuda,Seung Chik Jwa,Mikako Goto et al. Mariko Usuda et al.
To assess the risk of major birth defects after first-trimester exposure to carbocisteine and ambroxol during pregnancy, we conducted a prospective cohort study using counseling data for drug use during pregnancy provided by the Japan Drug ...