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Works by Shakarami, Fatemeh

Results: 3

1

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

By:

Shakarami, Fatemeh;
Nouri, Zahra;
Khanahmad, Hossein;
Ghazavi, Mohamadreza;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

2

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

By:

Shakarami, Fatemeh;
Jahani, Mehdi;
Nouri, Zahra;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

3

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

By:

Shakarami, Fatemeh;
Mohammad Taghi Akbari;
Shohreh Zare Karizi

Publication type:

Article