Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fatemeh Shakarami"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Background X‐linked mental retardation‐hypotonic facies syndrome‐1 (MRXFH1), caused by a mutation in the ATRX gene, is a rare syndromic form of X‐linked mental retardation (XLMR) that is mainly characterized by severe intellectual di
Externí odkaz:
https://doaj.org/article/925f65b536c6485ba12a20f03e0c292b
Publikováno v:
Iranian Journal of Reproductive Medicine, Vol 13, Iss 10, Pp 627-632 (2015)
Background: Recurrent pregnancy loss (RPL) defined by two or more failed pregnancies before 20 weeks of gestation. Several factors play a role in RPL including thrombophilic conditions which can be influenced by gene polymorphisms. Plasminogen activa
Externí odkaz:
https://doaj.org/article/2b0b88b8699741b1b3f269b0400f424d
Publikováno v:
Gene, Cell and Tissue. 3
Background: Recurrent pregnancy loss (RPL) is two or more consecutive pregnancy losses before 20 weeks of gestation. So far the disease is known for a variety of reasons, but still about 50% of recurrent pregnancy losses are unknown. The miRNAs are a
Autor:
Shakarami, Fatemeh1 (AUTHOR), Jahani, Mehdi1 (AUTHOR), Nouri, Zahra1,2 (AUTHOR), Tabatabaiefar, Mohammad Amin1,3,4 (AUTHOR) tabatabaiefar@med.mui.ac.ir
Publikováno v:
Molecular Genetics & Genomic Medicine. Oct2022, Vol. 10 Issue 10, p1-11. 11p.
Publikováno v:
Journal of Assisted Reproduction & Genetics; Jul2023, Vol. 40 Issue 7, p1533-1558, 26p
Publikováno v:
Iranian Journal of Reproductive Medicine. Oct2015, Vol. 13 Issue 10, p625-630. 6p.
Publikováno v:
Genomics & Genetics Weekly; 10/27/2023, p596-596, 1p