Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

405 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Soemedi R, Wilson IJ, Bentham J, Darlay R, Töpf A, Zelenika D, Cosgrove C, Setchfield K, Thornborough C, Granados-Riveron J, Blue GM, Breckpot J, Hellens S, Zwolinkski S, Glen E, Mamasoula C, Rahman TJ, Hall D, Rauch A, Devriendt K, Gewillig M, O' Sullivan J, Winlaw DS, Bu'Lock F, Brook JD, Bhattacharya S, Lathrop M, Santibanez-Koref M, Cordell HJ, Goodship JA, Keavney BD. Soemedi R, et al. Among authors: gewillig m. Am J Hum Genet. 2012 Sep 7;91(3):489-501. doi: 10.1016/j.ajhg.2012.08.003. Epub 2012 Aug 30. Am J Hum Genet. 2012. PMID: 22939634 Free PMC article.
Renal and urological tract malformations caused by a 22q11 deletion.
Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M. Devriendt K, et al. Among authors: gewillig m. J Med Genet. 1996 Apr;33(4):349. doi: 10.1136/jmg.33.4.349. J Med Genet. 1996. PMID: 8730297 Free PMC article. No abstract available.
Familial deletions of chromosome 22q11: the Leuven experience.
Swillen A, Devriendt K, Vantrappen G, Vogels A, Rommel N, Fryns JP, Eyskens B, Gewillig M, Dumoulin M. Swillen A, et al. Among authors: gewillig m. Am J Med Genet. 1998 Dec 28;80(5):531-2. Am J Med Genet. 1998. PMID: 9880224 No abstract available.
405 results