Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Magda A. Eshiesh"'
Publikováno v:
The Egyptian Heart Journal, Vol 70, Iss 4, Pp 267-270 (2018)
The 22q11.21 region is prone to low-copy repeats events that lead to congenital anomaly disorders. We tested genomic DNA of 20 families with non-syndromic CHD patients using a set of three known consecutive high polymorphic short tandem repeat (STR)
Externí odkaz:
https://doaj.org/article/2f418573b96247978b61d20a65d3ff8e
Publikováno v:
The Egyptian Heart Journal
The Egyptian Heart Journal, Vol 70, Iss 4, Pp 267-270 (2018)
The Egyptian Heart Journal, Vol 70, Iss 4, Pp 267-270 (2018)
The 22q11.21 region is prone to low-copy repeats events that lead to congenital anomaly disorders. We tested genomic DNA of 20 families with non-syndromic CHD patients using a set of three known consecutive high polymorphic short tandem repeat (STR)