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Items: 14

1.

Selenium and Iron Oxide Nanocomposites for Magnetically-Targeted Anti-Cancer Applications.

Hauksdóttir HL, Webster TJ.

J Biomed Nanotechnol. 2018 Mar 1;14(3):510-525. doi: 10.1166/jbn.2018.2521.

PMID:
29663923
2.

A de novo 1.13 Mb microdeletion in 12q13.13 associated with congenital distal arthrogryposis, intellectual disability and mild dysmorphism.

Jonsson DI, Ludvigsson P, Aradhya S, Sigurdardottir S, Steinarsdottir M, Hauksdottir H, Jonsson JJ.

Eur J Med Genet. 2012 Jun;55(6-7):437-40. doi: 10.1016/j.ejmg.2012.03.001. Epub 2012 Apr 2.

PMID:
22534424
3.

Monitoring, alarm, and data visualization service on sample preparing and sample storing devices in biobanks.

Hauksdóttir H, Jónsdóttir K, Thorarinsson A.

Methods Mol Biol. 2011;675:387-403. doi: 10.1007/978-1-59745-423-0_24.

PMID:
20949405
4.

Effect of hypoxia and TP53 mutation status and cytogenetics of normal and malignant mammary epithelium.

Vidarsson H, Steinarsdóttir M, Jónasson JG, Júlíusdóttir H, Hauksdóttir H, Hilmarsdóttir H, Halldórsdóttir K, Ogmundsdóttir HM.

Cancer Genet Cytogenet. 2006 Mar;165(2):144-50.

PMID:
16527608
5.

Functional analysis of the RING-type ubiquitin ligase family of Arabidopsis.

Stone SL, Hauksdóttir H, Troy A, Herschleb J, Kraft E, Callis J.

Plant Physiol. 2005 Jan;137(1):13-30.

6.

Cytogenetic changes in nonmalignant breast tissue.

Steinarsdóttir M, Jónasson JG, Vidarsson H, Júlíusdóttir H, Hauksdóttir H, Ogmundsdóttir HM.

Genes Chromosomes Cancer. 2004 Sep;41(1):47-55.

PMID:
15236316
8.
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10.

Active prevention in diabetic eye disease. A 4-year follow-up.

Kristinsson JK, Hauksdóttir H, Stefánsson E, Jónasson F, Gíslason I.

Acta Ophthalmol Scand. 1997 Jun;75(3):249-54.

11.

[Eye injuries in Icelandic children.].

Hauksdottir H, Sigurdsson H.

Laeknabladid. 1995 Dec;81(12):845-9. Icelandic.

PMID:
20065465
12.

Pericentric inversion of chromosome 13.

Hauksdóttir H, Arnardóttir A, Steinarsdóttir M, Gudmundsdóttir E, Halldórsson S, Gunnarsson A, Mikkelsen M.

J Med Genet. 1983 Apr;20(2):154-5. No abstract available.

13.

Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.

Hauksdóttir H, Halldórsson S, Jensson O, Mikkelsen M, McDermott A.

J Med Genet. 1972 Dec;9(4):413-21. No abstract available.

14.

45, X-46, XY chromosome mosaic with features of the Russell-Silver syndrome: a case report with a review of the literature.

Tulinius H, Tryggvason K, Hauksdottir H.

Dev Med Child Neurol. 1972 Apr;14(2):161-72. No abstract available.

PMID:
5063912

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