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Items: 3

1.

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family.

Nozari A, Aghaei-Moghadam E, Zeinaloo A, Alavi A, Ghasemi Firouzabdi S, Minaee S, Eskandari Hesari M, Behjati F.

Cell J. 2019 Apr;21(1):70-77. doi: 10.22074/cellj.2019.5734. Epub 2018 Nov 18.

PMID:
30507091
2.

A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family.

Nozari A, Aghaei-Moghadam E, Zeinaloo A, Mollazadeh R, Majnoon MT, Alavi A, Ghasemi Firouzabadi S, Mohammadzadeh A, Banihashemi S, Nikzaban M, Najmabadi H, Behjati F.

Gene. 2018 Jun 15;659:160-167. doi: 10.1016/j.gene.2018.03.044. Epub 2018 Mar 15.

PMID:
29551499
3.

Patent ductus arteriousus device closure in an infant with rubinstein-taybi syndrome.

Aghaei-Moghadam E, Zanjani KS, Ghandi Y.

Iran J Pediatr. 2013 Dec;23(6):708-9. No abstract available.

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