Works by Shakarami, Fatemeh
Results: 3
X‐linked mental retardation‐hypotonic facies syndrome: Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2034
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- Publication type:
- Article
A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review.
- Published in:
- Journal of Genetics, 2023, v. 102, n. 2, p. 1, doi. 10.1007/s12041-023-01441-x
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- Publication type:
- Article
Association of plasminogen activator inhibitor-1 (PAI-1) and angiotensin converting enzyme polymorphisms with recurrent pregnancy loss in Iranian women.
- Published in:
- Iranian Journal of Reproductive Medicine, 2015, v. 13, n. 10, p. 625
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- Publication type:
- Article