Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sayed Mohamed Hasan"'
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 3, Iss 2, Pp 108-112 (2020)
Background: Infantile systemic hyalinosis (ISH), an allelic form of hyaline fibromatosis syndrome, is a rare fatal autosomal recessive disorder that is caused by mutations in the CMG2/ANTRX2 gene encoding the transmembrane anthrax toxin receptor 2. I
Externí odkaz:
https://doaj.org/article/b7d9c2fc45c54dcf84ec69ee2b0faab0
Publikováno v:
Skeletal Radiology. 52:797-801
Publikováno v:
Journal of Biochemical and Clinical Genetics. :108-112
Background: Infantile systemic hyalinosis (ISH), an allelic form of hyaline fibromatosis syndrome, is a rare fatal autosomal recessive disorder that is caused by mutations in the CMG2/ANTRX2 gene encoding the transmembrane anthrax toxin receptor 2. I
Publikováno v:
SPIE Proceedings.
The article is devoted to lingual synergy based on the conceptions of complicated self-organizing systems development. Paper analyses entropic-and-information language characteristics built on the principles of determination and stochasticity. As a p