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Items: 5

1.

GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease.

Kalayinia S, Maleki M, Rokni-Zadeh H, Changi-Ashtiani M, Ahangar H, Biglari A, Shahani T, Mahdieh N.

J Clin Lab Anal. 2019 May 22:e22923. doi: 10.1002/jcla.22923. [Epub ahead of print]

PMID:
31115957
2.

Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report.

Kalayinia S, Shahani T, Biglari A, Maleki M, Rokni-Zadeh H, Razavi Z, Mahdieh N.

J Clin Lab Anal. 2019 Feb;33(2):e22663. doi: 10.1002/jcla.22663. Epub 2018 Sep 26.

PMID:
30259573
3.

Next generation sequencing applications for cardiovascular disease.

Kalayinia S, Goodarzynejad H, Maleki M, Mahdieh N.

Ann Med. 2018 Mar;50(2):91-109. doi: 10.1080/07853890.2017.1392595. Epub 2017 Oct 26.

PMID:
29027470
4.

Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosis.

Izadi F, Mahjoubi F, Farhadi M, Kalayinia S, Bidmeshkipour A, Tavakoli MM, Samanian S.

Indian J Med Res. 2016 Mar;143(3):303-7. doi: 10.4103/0971-5916.182620.

5.

Association between the atrial natriuretic peptide rs5065 gene polymorphism and the presence and severity of coronary artery disease in an Iranian population.

Ziaee S, Kalayinia S, Boroumand MA, Pourgholi L, Cheraghi S, Anvari MS, Sheikhvatan M.

Coron Artery Dis. 2014 May;25(3):242-6. doi: 10.1097/MCA.0000000000000075.

PMID:
24487939

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