Zobrazeno 1 - 2
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pro vyhledávání: '"Ying-Yen Weng"'
Autor:
Yen-Hui Chiu, Yu-Ning Liu, Hsiao-Jan Chen, Ying-Chen Chang, Shu-Min Kao, Mei-Ying Liu, Ying-Yen Weng, Kwang-Jen Hsiao, Tze-Tze Liu
Publikováno v:
Data in Brief, Vol 25, Iss , Pp - (2019)
Glucose-6-phosphate dehydrogenase deficiency (G6PD deficiency; OMIM #300908) is the most common inborn error disorders worldwide. While the G6PD is the key enzyme of removing oxidative stress in erythrocytes, the early diagnosis is utmost vital to pr
Externí odkaz:
https://doaj.org/article/f0d1f512adb44c389c8e1d11b0f4a8cf
Publikováno v:
Journal of molecular medicine (Berlin, Germany). 79(5-6)
Congenital defects in human chromosome 22q11 deletion syndromes are associated with the 3rd and 4th pharyngeal pouch during fetal development. In the cardiovascular system, these disorders are usually apparent as conotruncal heart defects and aortic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df191877220504fd5c07b6d29086b52f
https://pubmed.ncbi.nlm.nih.gov/11485030
https://pubmed.ncbi.nlm.nih.gov/11485030