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Items: 4

1.

Association of cytokine gene polymorphisms with osteoarthritis susceptibility.

Rogoveanu OC, Calina D, Cucu MG, Burada F, Docea AO, Sosoi S, Stefan E, Ioana M, Burada E.

Exp Ther Med. 2018 Sep;16(3):2659-2664. doi: 10.3892/etm.2018.6477. Epub 2018 Jul 18.

2.

A rare occurrence of three consecutive autosomal trisomic pregnancies in a couple without offspring.

Burada F, Sosoi S, Iliescu D, Ioana M, Cernea D, Tudorache S.

Clin Exp Obstet Gynecol. 2016;43(2):287-90.

PMID:
27132432
3.

Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31.

Sosoi S, Streata I, Tudorache S, Burada F, Siminel M, Cernea N, Ioana M, Iliescu DG, Mixich F.

J Hum Genet. 2015 Apr;60(4):183-5. doi: 10.1038/jhg.2015.4. Epub 2015 Feb 5.

PMID:
25652353
4.

Terminal deletion 2q37.3 in a patient with Klippel-Trenaunay-Weber syndrome.

Puiu I, Stoica A, Sosoi S, Puiu A, Ioana M, Burada F.

Fetal Pediatr Pathol. 2013 Oct;32(5):351-6. doi: 10.3109/15513815.2013.768739. Epub 2013 Feb 25.

PMID:
23438794

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